Leber congenital amaurosis 12

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

Also known as: LCA12, Leber congenital amaurosis 12, Leber congenital amaurosis caused by mutation in RD3, Leber congenital amaurosis type 12, RD3 Leber congenital amaurosis, amaurosis congenita of Leber, type 12

33 clinical trials for this condition and its sub-types.