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
03176 CORD12 dystrophy, cone-rod, type 12 (CORD-12) 612657 AD;AR - - PROM1 - -
02732 MCDR2 dystrophy, macular, retinal, type 2 (MCDR2, Bull's eye macular dystrophy) 608051 AD 3 3 PROM1 - -
03087 RP41 retinitis pigmentosa, type 41 (RP41) 612095 AR 2 2 PROM1 - -
06107 RP7 retinitis pigmentosa 7, digenic form 608133 AD;AR - - ROM1 - -
02467 STGD4 Stargardt disease, type 4 (STGD-4) 603786 AD 4 4 PROM1 - -
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