Congenital stationary night blindness autosomal dominant 1

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

Also known as: CSNBAD1, RHO congenital stationary night blindness, congenital stationary night blindness autosomal dominant type 1, congenital stationary night blindness caused by mutation in RHO, night blindness, congenital stationary, autosomal dominant type 1, night blindness, congenital stationary, autosomal dominant 1, night blindness, congenital stationary, rhodopsin-related

49 clinical trials for this condition and its sub-types, 3 tagged with Congenital stationary night blindness autosomal dominant 1 itself.