Leber congenital amaurosis 5

Any Leber congenital amaurosis in which the cause of the disease is a mutation in the LCA5 gene.

Also known as: LCA5, LCA5 Leber congenital amaurosis, Leber congenital amaurosis 5, Leber congenital amaurosis caused by mutation in LCA5, Leber congenital amaurosis type 5, amaurosis congenita of Leber, type 5

27 clinical trials for this condition and its sub-types, 2 tagged with Leber congenital amaurosis 5 itself.