Leber congenital amaurosis 9

Any Leber congenital amaurosis in which the cause of the disease is a mutation in the NMNAT1 gene.

Also known as: LCA9, Leber congenital amaurosis 9, Leber congenital amaurosis caused by mutation in NMNAT1, Leber congenital amaurosis type 9, NMNAT1 Leber congenital amaurosis, amaurosis congenita of Leber, type 9

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