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Results 1 - 5 of 5 for "X-linked" retinitis pigmentosa
  1. RPGR gene 
    ... for about 70 percent of all cases of X-linked retinitis pigmentosa.Most of the mutations responsible for X-linked retinitis pigmentosa occur in the ORF15 exon of the RPGR ...
    https://medlineplus.gov/genetics/gene/rpgr - Genetics
  2. RP2 gene 
    ... 10 to 15 percent of all cases of X-linked retinitis pigmentosa.Most mutations in the RP2 gene lead to ... in a North American cohort of families with X-linked retinitis pigmentosa. Am J Hum Genet. 2002 Jun;70(6): ...
    https://medlineplus.gov/genetics/gene/rp2 - Genetics
  3. Retinitis pigmentosa 
    ... 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 ...
    https://medlineplus.gov/genetics/condition/retinitis-pigmentosa - Genetics
  4. Nearsightedness 
    ... 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 ...
    https://medlineplus.gov/genetics/condition/nearsightedness - Genetics
  5. Cone-rod dystrophy 
    ... of rod-cone dystrophy is a condition called retinitis pigmentosa. ABCA4 CACNA1F CNGA3 CNGB3 CRB1 CRX GUCY2D PDE6C ...
    https://medlineplus.gov/genetics/condition/cone-rod-dystrophy - Genetics