Leber congenital amaurosis 15

Any Leber congenital amaurosis in which the cause of the disease is a mutation in the TULP1 gene.

Also known as: LCA15, Leber congenital amaurosis 15, Leber congenital amaurosis caused by mutation in TULP1, Leber congenital amaurosis type 15, TULP1 Leber congenital amaurosis, retinitis pigmentosa, juvenile, Tulp1-related

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