Congenital stationary night blindness 1F

Any congenital stationary night blindness in which the cause of the disease is a mutation in the LRIT3 gene.

Also known as: CSNB1F, LRIT3 congenital stationary night blindness, congenital stationary night blindness caused by mutation in LRIT3, congenital stationary night blindness type 1F, night blindness, congenital stationary (complete), 1F, autosomal recessive, night blindness, congenital stationary, type 1F

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