Leber congenital amaurosis 13

MONDO:0012990

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

Also known as: LCA13, Leber congenital amaurosis 13, Leber congenital amaurosis caused by mutation in RDH12, Leber congenital amaurosis type 13, RDH12 Leber congenital amaurosis, retinitis pigmentosa 53

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