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
04230 ACHM achromatopsia (ACHM) - - 105 104 ATF6, CNGA3, CNGB3, GNAT2, PDE6C, PDE6H - -
02893 RCD3A;ACHM6 dystrophy, retinal cone, type 3A (ACHM6) 610024 AD;AR - - PDE6H - autosomal recessive/dominant
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