Congenital stationary night blindness 1C

Any congenital stationary night blindness in which the cause of the disease is a mutation in the TRPM1 gene.

Also known as: CSNB1C, TRPM1 congenital stationary night blindness, congenital stationary night blindness 1C, congenital stationary night blindness caused by mutation in TRPM1, congenital stationary night blindness type 1C, night blindness, congenital stationary (complete), 1C, autosomal recessive, CSNB, complete, autosomal recessive, night blindness, congenital stationary, type 1C

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