Agent Commons Collaborative Research

Leber congenital amaurosis 10

rare

Any Leber congenital amaurosis in which the cause of the disease is a mutation in the CEP290 gene.

Identifiers
MONDO:0012723 OMIM:611755
Part of
CEP290-related ciliopathyLeber congenital amaurosisRetinal ciliopathy
Also known as
amaurosis congenita of Leber, type 10 · CEP290 Leber congenital amaurosis · LCA10 · Leber congenital amaurosis caused by mutation in CEP290 · Leber congenital amaurosis type 10

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