All diseases

3 entries on 1 page. Showing entries 1 - 3.
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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 - -
05432 PFIC cholestasis, intrahepatic, familial, progressive (PFIC) - - 8 5 ABCB11, ABCB4, ATP8B1, NR1H4, TJP2 - -
05033 PFIC4 cholestasis, intrahepatic, familial, progressive, type 4 (PFIC-4) 615878 AR 6 2 TJP2 - -
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