Leber congenital amaurosis 10

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

Also known as: CEP290 Leber congenital amaurosis, LCA10, Leber congenital amaurosis 10, Leber congenital amaurosis caused by mutation in CEP290, Leber congenital amaurosis type 10, amaurosis congenita of Leber, type 10

27 clinical trials for this condition and its sub-types, 2 tagged with Leber congenital amaurosis 10 itself.