retinitis pigmentosa 4

A retinitis pigmentosa that has_material_basis_in mutation in the RHO gene on chromosome 3q22.

congenital stationary night blindness autosomal dominant 1

A congenital stationary night blindness characterized by autosomal dominant inheritance that has_material_basis_in mutations in the RHO gene on chromosome 3q22.1.

hemolytic disease of the fetus

A microcytic anemia that is characterized by Rho(D) incompatibility, which may develop when a woman with Rh-negative blood is impregnated by an individual with Rh-positive blood and conceives a fetus with Rh-positive blood, sometimes resulting in hemolysis.