Human genes for congenital stationary night blindness autosomal dominant 2
Congenital stationary night blindness autosomal dominant 2 [DOID:0110863]
A congenital stationary night blindness characterized by autosomal dominant inhertance that has_material_basis_in heterozygous mutation in the PDE6B gene on chromosome 4p16.
Synonyms: congenital stationary night blindness autosomal dominant 2, DOID:0110863, CSNBAD2, Rambusch type congenital stationary night blindness, Rambusch type congenital stationary night blindnesses