/Leber congenital amaurosis 13

Leber congenital amaurosis 13

Rare Disease

MONDO:0012990

Also Known As

LCA13Leber congenital amaurosis 13Leber congenital amaurosis caused by mutation in RDH12Leber congenital amaurosis type 13RDH12 Leber congenital amaurosisretinitis pigmentosa 53

Definition

Any Leber congenital amaurosis in which the cause of the disease is a mutation in the RDH12 gene.

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Associated Genes

RDH12 ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:612712 ↗

GARD

GARD:10882 ↗

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