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
02701 FHCA hypercholanemia, familial (FHCA) 607748 AR - - BAAT, EPHX1, TJP2 - -
01587 PEE1 preeclampsia/eclampsia, type 1 (PEE-1) 189800 AD - - EPHX1, NOS3 - -
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