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
04230 ACHM achromatopsia (ACHM) - - 105 104 ATF6, CNGA3, CNGB3, GNAT2, PDE6C, PDE6H - -
02016 ACHM3 achromatopsia, type 3 262300 AR 35 34 CNGB3 - -
00420 STGD1 Stargardt disease, type 1 (STGD1) 248200 AR 3224 3092 ABCA4, CNGB3 - -
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