All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01269 DMBCYP2A6 metabolism, drug, resistance, coumarin 122700 AD 7 7 CYP2A6, CYP2C9, F9, VKORC1 - autosomal dominant
00139 ID intellectual disability (ID) - - 2792 2473 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 556 more - -
00550 MGORS1 Meier-Gorlin syndrome, type 1 (MGORS-1) 224690 AR - - ORC1 - -
02660 VKCFD2 vitamin K-dependent clotting factors, combined deficiency of, type 2 (VKCFD-2) 607473 - 2 2 VKORC1 - -
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