/congenital stationary night blindness autosomal dominant 2
congenital stationary night blindness autosomal dominant 2
Rare Disease
MONDO:0008099
Also Known As
CSNBAD2PDE6B congenital stationary night blindnessRambusch type congenital stationary night blindnesscongenital stationary night blindness autosomal dominant type 2congenital stationary night blindness caused by mutation in PDE6Bnight blindness, congenital stationary, autosomal dominant type 2night blindness, congenital stationary, Rambusch typenight blindness, congenital stationary, autosomal dominant 2
Definition
Any congenital stationary night blindness in which the cause of the disease is a mutation in the PDE6B gene.
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