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Results 1 - 6 of 6 for Achromatopsia 9
  1. Achromatopsia 
    ... j.ophtha.2009.03.053. Epub 2009 Jul 9. Citation on PubMed
    https://medlineplus.gov/genetics/condition/achromatopsia - Genetics
  2. OPN1SW gene 
    ... sensitive cone pigment gene associated with a tritan color vision defect. Vis Neurosci. 2006 May-Aug;23(3-4):403-9. doi: 10.1017/S0952523806233169. Citation on PubMed Neitz ...
    https://medlineplus.gov/genetics/gene/opn1sw - Genetics
  3. CNGB3 gene 
    ... cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to chromosome 8q21. Hum Mol Genet. 2000 Sep 1;9(14):2107-16. doi: 10.1093/hmg/9. ...
    https://medlineplus.gov/genetics/gene/cngb3 - Genetics
  4. GNAT2 gene 
    ... Maher ER. Mapping of a novel locus for achromatopsia (ACHM4) to 1p and identification of a germline mutation in the alpha subunit of cone transducin (GNAT2). J Med Genet. 2002 Sep;39(9):656-60. doi: 10.1136/jmg.39.9. ...
    https://medlineplus.gov/genetics/gene/gnat2 - Genetics
  5. CNGA3 gene 
    ... channel. Hum Mutat. 2010 Jul;31(7):830-9. doi: 10.1002/humu.21283. Citation on PubMed Kohl S, Jagle H, Wissinger B, Zobor D. Achromatopsia. 2004 Jun 24 [updated 2018 Sep 20]. In: ...
    https://medlineplus.gov/genetics/gene/cnga3 - Genetics
  6. Farsightedness 
    ... with farsightedness as a characteristic feature include microphthalmia, achromatopsia, aniridia, Leber congenital amaurosis, X-linked juvenile retinoschisis, ...
    https://medlineplus.gov/genetics/condition/farsightedness - Genetics