Congenital stationary night blindness 1D

Any congenital stationary night blindness in which the cause of the disease is a mutation in the SLC24A1 gene.

Also known as: CSNB1D, SLC24A1 congenital stationary night blindness, congenital stationary night blindness 1D, congenital stationary night blindness caused by mutation in SLC24A1, congenital stationary night blindness type 1D, night blindness, congenital stationary (complete), 1D, autosomal recessive, Csnb, complete, autosomal recessive, night blindness, congenital stationary, type 1D

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