All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00347 ARMD macular degeneration, age-related (ARMD) - - 30 34 ABCA4, CFH, FBLN5, HMCN1 - -
01425 ARMD2 macular degeneration, age-related, type 2 (ARMD-2) 153800 AD 1 1 ABCA4 - -
00421 CORD3 dystrophy, cone rod, type 3 (CORD-3) 604116 - 15 13 ABCA4 - -
02387 RP19 retinitis pigmentosa, type 19 (RP19) 601718 AR 8 6 ABCA4 - -
00420 STGD1 Stargardt disease, type 1 (STGD1) 248200 AR 3224 3092 ABCA4, CNGB3 - -
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