Congenital stationary night blindness 1F
Congenital stationary night blindness 1F
Definition
Any congenital stationary night blindness in which the cause of the disease is a mutation in the LRIT3 gene.
Also known as congenital stationary night blindness caused by mutation in LRIT3, congenital stationary night blindness type 1F, CSNB1F, LRIT3 congenital stationary night blindness, night blindness, congenital stationary (complete), 1F, autosomal recessive — per MONDO