All diseases

6 entries on 1 page. Showing entries 1 - 6.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
06327 CACD1 ?Choroidal dystrophy, central areolar 1 215500 AD - - GUCY2D - -
00058 CORD dystrophy, cone-rod (CORD) - - 363 361 ADAM9, DRAM2, GUCY2D, PITPNM3, POC1B, RAB28, TTLL5 - -
02389 CORD6 dystrophy, cone-rod, type 6 (CORD-6) 601777 AD;AR - - GUCY2D - -
06381 CSNB1I Night blindness, congenital stationary, type 1I 618555 AR - - GUCY2D - -
04210 LCA Leber congenital amaurosis (LCA) - - 1137 1109 GDF6, GUCY2D, NMNAT1 - -
01646 LCA1 Leber congenital amaurosis, type 1 (LCA-1) 204000 AR - - GUCY2D - -
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