Leber congenital amaurosis 14

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

Also known as: LCA14, LRAT Leber congenital amaurosis, Leber congenital amaurosis 14, Leber congenital amaurosis caused by mutation in LRAT, Leber congenital amaurosis type 14, retinal dystrophy, early-onset severe, retinal dystrophy, early-onset Severe, LRAT-related, retinitis pigmentosa, juvenile

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