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

25 clinical trials for this condition and its sub-types, 0 tagged with Leber congenital amaurosis 13 itself.

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↑ Leber congenital amaurosis (13) ↑ RDH12-related recessive retinopathy (0)

Including sub-types (25) Tagged with Leber congenital amaurosis 13 (0)

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