Congenital stationary night blindness 1H

Any congenital stationary night blindness in which the cause of the disease is a mutation in the GNB3 gene.

Also known as: CSNB1H, GNB3 congenital stationary night blindness, congenital stationary night blindness caused by mutation in GNB3, congenital stationary night blindness type 1H, night blindness, congenital stationary, type 1H

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