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
03460 LCA15 Leber congenital amaurosis, type 15 (LCA-15) 613843 AR 12 8 TULP1 - -
02289 RP14 retinitis pigmentosa, type 14 (RP14) 600132 AR 1 1 TULP1 - -
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