All diseases

2 entries on 1 page. Showing entries 1 - 2.
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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
02660 VKCFD2 vitamin K-dependent clotting factors, combined deficiency of, type 2 (VKCFD-2) 607473 - 2 2 VKORC1 - -
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