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
03457 LCA11 Leber congenital amaurosis, type 11 (LCA-11) 613837 - - - IMPDH1 - -
01543 RP10 retinitis pigmentosa, type 10 (RP10) 180105 AD - - IMPDH1 - -
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