Leber congenital amaurosis 6

Any Leber congenital amaurosis in which the cause of the disease is a mutation in the RPGRIP1 gene.

Also known as: LCA6, Leber congenital amaurosis 6, Leber congenital amaurosis caused by mutation in RPGRIP1, Leber congenital amaurosis type 6, RPGRIP1 Leber congenital amaurosis

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