All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03182 LCA13;RP53 Leber congenital amaurosis, type 13 (LCA13, retinitis pigmentosa, type 53 (RP53)) 612712 AD;AR 2 2 RDH12 - -
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