Leber congenital amaurosis 17

Any Leber congenital amaurosis in which the cause of the disease is a mutation in the GDF6 gene.

Also known as: GDF6 Leber congenital amaurosis, LCA17, Leber congenital amaurosis 17, Leber congenital amaurosis caused by mutation in GDF6, Leber congenital amaurosis type 17

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