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"X-linked" "cone-rod" dystrophy 3
- ... linked cone-rod dystrophy 1 Genetic Testing Registry: X-linked cone-rod dystrophy 3 Cone rod dystrophy National Organization for Rare Disorders ( ... CONE-ROD DYSTROPHY 1; CORD1 CONE-ROD DYSTROPHY, X-LINKED, 3; CORDX3 CONE-ROD DYSTROPHY 6; CORD6 CONE-ROD DYSTROPHY, X-LINKED, 1; ...
- ... and RP2 genes account for most cases of X-linked retinitis pigmentosa.The genes associated with retinitis pigmentosa play essential ... an X-linked pattern. The genes associated with X-linked retinitis pigmentosa are located on the X chromosome, which is ...
- ... conditions include autosomal recessive congenital stationary night blindness, X-linked congenital stationary night blindness, Stickler syndrome, Marfan syndrome, retinitis pigmentosa, cone-rod dystrophy, deafness and myopia syndrome, Knobloch ...