Congenital stationary night blindness autosomal dominant 2

MONDO:0008099

Any congenital stationary night blindness in which the cause of the disease is a mutation in the PDE6B gene.

Also known as: CSNBAD2, PDE6B congenital stationary night blindness, congenital stationary night blindness autosomal dominant type 2, congenital stationary night blindness caused by mutation in PDE6B, night blindness, congenital stationary, autosomal dominant type 2, night blindness, congenital stationary, Rambusch type, night blindness, congenital stationary, autosomal dominant 2

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