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Results 1 - 10 of 11 for "X-linked" "cone-rod" dystrophy 3
  1. Cone-rod dystrophy 
    ... 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; ...
    https://medlineplus.gov/genetics/condition/cone-rod-dystrophy - Genetics
  2. RP2 gene 
    ... in a North American cohort of families with X-linked retinitis pigmentosa. Am J Hum Genet. 1999 Mar;64(3):897-900. doi: 10.1086/302298. No abstract available. Citation on PubMed or Free article on PubMed Central ... the gene for X-linked retinitis pigmentosa 2. Nat Genet. 1998 Aug;19(4):327- ...
    https://medlineplus.gov/genetics/gene/rp2 - Genetics
  3. RPGR gene 
    ... body. COD1 CORDX1 CRD PCDX retinitis pigmentosa 15 retinitis pigmentosa 3 GTPase regulator RP15 RP3 RPGR_HUMAN X-linked retinitis pigmentosa GTPase regulator XLRP3 Tests of RPGR ...
    https://medlineplus.gov/genetics/gene/rpgr - Genetics
  4. CACNA1F gene 
    ... J, Sankila EM, Alitalo T, Bech-Hansen NT. X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the ... L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness. Nat Genet. 1998 Jul;19(3):260-3. doi: 10.1038/940. Citation on ...
    https://medlineplus.gov/genetics/gene/cacna1f - Genetics
  5. 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
  6. 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
  7. Retinitis Pigmentosa (Foundation Fighting Blindness)  
    Usher Syndrome/Learn More ... Usher Syndrome ... Retinal Disorders/Specifics ... Retinal Disorders ... Foundation Fighting Blindness ... What is Retinitis Pigmentosa? Learn about ...
    https://www.fightingblindness.org/diseases/retinitis-pigmentosa - External Health Links
  8. Bardet-Biedl Syndrome (Foundation Fighting Blindness)  
    Retinal Disorders/Specifics ... Retinal Disorders ... Birth Defects/Specifics ... Birth Defects ... What is Bardet Biedl Syndrome? Learn about the signs and symptoms of the ...
    https://www.fightingblindness.org/diseases/bardet-biedl-syndrome-bbs - External Health Links
  9. Choroideremia (Foundation Fighting Blindness)  
    Eye Diseases/Specifics ... Eye Diseases ... Retinal Disorders/Specifics ... Retinal Disorders ... Foundation Fighting Blindness ... What is Choroideremia? Learn about the signs ...
    https://www.fightingblindness.org/diseases/choroideremia - External Health Links
  10. Muscular Dystrophy From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Muscular Dystrophy/Start Here ... Muscular Dystrophy ... National Institute of Neurological Disorders and Stroke ... Muscular dystrophy (MD) refers to a group of genetic ...
    https://www.ninds.nih.gov/.../disorders/muscular-dystrophy - External Health Links
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