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
00468 FPH hyperpigmentation, progressive, familial (FPH) 145250 - - - KITLG - -
00466 SHEP-7 pigmentation, hair, blond/brown, type 7 (SHEP-7, skin/hair/eye pigmentation) 611664 - - - KITLG - -
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