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
06168 DFNA69 Deafness, autosomal dominant 69, unilateral or asymmetric 616697 AD - - KITLG - -
00468 FPHH hyperpigmentation, progressive, familial (FPHH) 145250 AD 1 1 KITLG - -
00466 SHEP7 pigmentation, hair, blond/brown, type 7 (SHEP-7, skin/hair/eye pigmentation) 611664 - 1 1 KITLG - -
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