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
04210 LCA Leber congenital amaurosis (LCA) - - 1137 1109 GDF6, GUCY2D, NMNAT1 - -
00219 LCA9 Leber congenital amaurosis, type 9 (LCA-9) 608553 AR 67 22 NMNAT1 - -
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