All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00112 RP retinitis pigmentosa (RP) 268000 - 218 144 ARL3, BEST1, CC2D2A, CNGB1, DHDDS, HKDC1, IDH3A, IMPG1, KIF3B, NR2E3, SLC7A14 - -
06963 RP91 retinitis pigmentosa, type 91 153870 AD - - IMPG1 - -
01424 VMD dystrophy, macular, vitelliform (VMD) - - 6 3 BEST1, IMPG1, IMPG2, PRPH2 - -
04518 VMD4 dystrophy, macular, vitelliform, type 4 (VMD-4) 616151 AD - - IMPG1 - -
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