Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 5 of 5 for Cone dystrophy "5," "X-linked"
  1. Cone-rod dystrophy 
    ... DYSTROPHY, X-LINKED, 1; CORDX1 CONE-ROD DYSTROPHY 5; CORD5 CONE-ROD DYSTROPHY, X-LINKED, 2; CORDX2 CONE-ROD DYSTROPHY 7; CORD7 CONE- ...
    https://medlineplus.gov/genetics/condition/cone-rod-dystrophy - Genetics
  2. RPGR gene 
    ... Zhang K. Mutations in the RPGR gene cause X-linked cone dystrophy. Hum Mol Genet. 2002 Mar 1;11(5):605-11. doi: 10.1093/hmg/11.5. ...
    https://medlineplus.gov/genetics/gene/rpgr - Genetics
  3. CACNA1F gene 
    ... J, Sankila EM, Alitalo T, Bech-Hansen NT. X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the ...
    https://medlineplus.gov/genetics/gene/cacna1f - 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 syndrome, and Cohen ...
    https://medlineplus.gov/genetics/condition/nearsightedness - Genetics
  5. Color vision deficiency 
    ... OPN1SW Red-green color vision defects and blue cone monochromacy are inherited in an X-linked recessive pattern. The OPN1LW and OPN1MW genes are ... human color vision. Clin Genet. 2005 May;67(5):369-77. doi: ... cone monochromacy: causative mutations and associated phenotypes. Mol Vis. ...
    https://medlineplus.gov/genetics/condition/color-vision-deficiency - Genetics