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Results 1 - 6 of 6 for "X-linked" "cone-rod" dystrophy 1
  1. Cone-rod dystrophy 
    ... Testing Registry: Cone-rod dystrophy Genetic Testing Registry: X-linked cone-rod dystrophy 1 Genetic Testing Registry: X-linked cone-rod dystrophy ... CONE-ROD DYSTROPHY 6; CORD6 CONE-ROD DYSTROPHY, X-LINKED, 1; CORDX1 CONE-ROD DYSTROPHY 5; CORD5 CONE-ROD DYSTROPHY, X-LINKED, 2; ...
    https://medlineplus.gov/genetics/condition/cone-rod-dystrophy - Genetics
  2. RPGR gene 
    ... WITHOUT DEAFNESS; RPSRDF RETINITIS PIGMENTOSA GTPase REGULATOR; RPGR CONE-ROD DYSTROPHY, X-LINKED, 1; CORDX1 NCBI Gene ClinVar Ayyagari R, Demirci FY, ...
    https://medlineplus.gov/genetics/gene/rpgr - Genetics
  3. RP2 gene 
    ... the primary cilium. Hum Mol Genet. 2010 Apr 1;19(7):1358-67. doi: ... X-linked retinitis pigmentosa protein RP2, its homologue cofactor C and the ...
    https://medlineplus.gov/genetics/gene/rp2 - 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 ... 1007/s00424-021-02570-x. Epub 2021 Jul 1. Citation on PubMed MacDonald IM, Hoang S, Tuupanen S. X-Linked Congenital Stationary Night Blindness. 2008 Jan 16 [updated ...
    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 
    ... ClinicalTrials.gov MYOPIA 2, AUTOSOMAL DOMINANT; MYP2 MYOPIA 1, X-LINKED; MYP1 MYOPIA 13, X-LINKED; MYP13 MYOPIA 18, ...
    https://medlineplus.gov/genetics/condition/nearsightedness - Genetics