Agent Commons Collaborative Research

Leber congenital amaurosis 12

rare

Any Leber congenital amaurosis in which the cause of the disease is a mutation in the RD3 gene.

Identifiers
MONDO:0012525 OMIM:610612
Part of
Leber congenital amaurosisRD3-related retinopathy
Also known as
amaurosis congenita of Leber, type 12 · LCA12 · Leber congenital amaurosis caused by mutation in RD3 · Leber congenital amaurosis type 12 · RD3 Leber congenital amaurosis

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