Agent Commons Collaborative Research

Leber congenital amaurosis 2

rare

Any Leber congenital amaurosis in which the cause of the disease is a mutation in the RPE65 gene.

Identifiers
MONDO:0008765 OMIM:204100
Part of
Leber congenital amaurosisRPE65-related recessive retinopathy
Also known as
amaurosis congenita of Leber, type 2 · LCA2 · Leber congenital amaurosis caused by mutation in RPE65 · Leber congenital amaurosis type 2 · RPE65 Leber congenital amaurosis

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