Human genes for Oguchi disease-2
Oguchi disease-2 [DOID:0110713]
A congenital stationary night blindness characterized by congenital static night blindness, a golden or gray-white discoloration of the fundus that disappears in the dark-adapted state and typically normal function of all other visual functions that has_material_basis_in homozygous mutation in the GRK1 gene on chromosome 13q34.
Synonyms: Oguchi disease-2, DOID:0110713, Oguchi disease2, congenital stationary night blindness Oguchi type 2, CSNBO2