Congenital stationary night blindness 1E

MONDO:0013807

Any congenital stationary night blindness in which the cause of the disease is a mutation in the GPR179 gene.

Also known as: CSNB1E, GPR179 congenital stationary night blindness, congenital stationary night blindness 1E, congenital stationary night blindness caused by mutation in GPR179, congenital stationary night blindness type 1E, night blindness, congenital stationary (complete), 1E, autosomal recessive, Csnb, complete, autosomal recessive, night blindness, congenital stationary, type 1E

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