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
03365 RP56 retinitis pigmentosa, type 56 (RP56, maculopathy) 613581 AR 0 0 IMPG2 - -
01424 VMD dystrophy, macular, vitelliform (VMD) - - 3 0 BEST1, IMPG1, IMPG2, PRPH2 - -
04519 VMD5 dystrophy, macular, vitelliform, type 5 (VMD-5) 616152 AD 1 1 IMPG2 - -
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