Congenital stationary night blindness 1B

Any congenital stationary night blindness in which the cause of the disease is a mutation in the GRM6 gene.

Also known as: CSNB1B, GRM6 congenital stationary night blindness, congenital stationary night blindness 1B, congenital stationary night blindness caused by mutation in GRM6, congenital stationary night blindness type 1B, night blindness, congenital stationary (complete), 1B, autosomal recessive, CSNB, complete, autosomal recessive, night blindness, congenital stationary, complete, autosomal recessive

46 clinical trials for this condition and its sub-types, 0 tagged with Congenital stationary night blindness 1B itself.