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
01647 LCA2 Leber congenital amaurosis, type 2 (LCA-2) 204100 AR 29 29 RPE65 - -
03436 RP20 retinitis pigmentosa, type 20 (RP20) 613794 AR 0 0 RPE65 - -
05702 RP87 retinitis pigmentosa, type 87, choroidal involvement (RP87) 618697 AD 0 0 RPE65 - -
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