All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00058 CORD dystrophy, cone-rod (CORD) - - 355 355 ADAM9, GUCY2D, PITPNM3, POC1B, RAB28, TTLL5 - -
04618 CORD20 dystrophy, cone-rod, type 20 (CORD20) 615973 AR 2 2 POC1B - -
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