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 11 - 20 of 31 for "Cone-rod" dystrophy 5
  1. TRNT1 deficiency 
    ... approximately every 2 to 4 weeks and lasting 5 to 7 days, although the frequency ... called retinitis pigmentosa, in which the light-sensing cells of the ...
    https://medlineplus.gov/genetics/condition/trnt1-deficiency - Genetics
  2. Neuropathy, ataxia, and retinitis pigmentosa 
    Neuropathy, ataxia, and retinitis pigmentosa (NARP) is a condition that causes a variety of signs and symptoms that mainly affect the nervous system. The condition ...
    https://medlineplus.gov/...europathy-ataxia-and-retinitis-pigmentosa - Genetics
  3. RPGR gene 
    ... 5):605-11. doi: 10.1093/hmg/11.5.605. Citation on PubMed Zito I, ... pigmentosa, impaired hearing, and sinorespiratory infections. J Med Genet. ...
    https://medlineplus.gov/genetics/gene/rpgr - Genetics
  4. CLRN1 gene 
    ... In: Am J Hum Genet 2001 Nov;69(5):1160. Citation on PubMed or Free article on ... nonsyndromic retinitis pigmentosa. Ophthalmology. 2011 Jul;118(7):1444-8. doi: ...
    https://medlineplus.gov/genetics/gene/clrn1 - Genetics
  5. USH2A gene 
    ... doi: 10.1073/pnas.0610950104. Epub 2007 Mar 5. Citation on PubMed or Free ... type II or non-syndromic retinitis pigmentosa. J Med Genet. 2010 Jul;47(7):499- ...
    https://medlineplus.gov/genetics/gene/ush2a - Genetics
  6. TRNT1 gene 
    ... 1182/blood-2014-08-591370. Epub 2014 Sep 5. Citation on PubMed or Free article ... retinitis pigmentosa with erythrocytic microcytosis. Hum Mol Genet. 2016 Jan ...
    https://medlineplus.gov/genetics/gene/trnt1 - Genetics
  7. CACNA1F gene 
    ... This Health Condition MedlinePlus Genetics provides information about Cone-rod dystrophy More About This Health Condition Variants in the ... 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
  8. Nearsightedness 
    ... 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
  9. Bardet-Biedl syndrome 
    ... extensively heterogeneous disease. Hum Genet. 2010 Mar;127(5):583-93. doi: 10.1007/s00439-010-0804- ...
    https://medlineplus.gov/genetics/condition/bardet-biedl-syndrome - Genetics
  10. MYO7A gene 
    ... were thought to have nonsyndromic hearing loss developed retinitis pigmentosa (a vision disorder characteristic of Usher syndrome) later ... However, other individuals diagnosed with DFNB2 never develop retinitis pigmentosa, and recent studies indicate that DFNB2 and Usher ...
    https://medlineplus.gov/genetics/gene/myo7a - Genetics
previous · 1 · 2 · 3 · 4 · next