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
01339 - fundus albipunctatus (retinitis punctata albescens (RPA)) 136880 AD;AR 110 110 PRPH2, RDH5, RHO, RLBP1 - -
03257 CACD2 dystrophy, choroidal, areolar, central, type 2 (CACD2) 613105 AD 3 - PRPH2 - -
01494 MDPT1 dystrophy, macular, patterned, type 1 (MDPT-1) 169150 AD - - PRPH2 - -
01424 VMD dystrophy, macular, vitelliform (VMD) - - 8 7 BEST1, IMPG1, IMPG2, PRPH2 - -
02739 VMD3 dystrophy, macular, vitelliform, type 3 (VMD-3) 608161 AD 1 1 PRPH2 - -
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