Leber congenital amaurosis 11

Any Leber congenital amaurosis in which the cause of the disease is a mutation in the IMPDH1 gene.

Also known as: IMPDH1 Leber congenital amaurosis, LCA11, Leber congenital amaurosis 11, Leber congenital amaurosis caused by mutation in IMPDH1, Leber congenital amaurosis type 11, amaurosis congenita of Leber, type 11

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