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 - 10 of 20 for "Cone-rod" dystrophy 1
  1. Cone-rod dystrophy 
    ... cone-rod dystrophy Tapetoretinal degeneration Genetic Testing Registry: Cone-rod dystrophy 1 Genetic Testing Registry: Cone-rod dystrophy 10 Genetic ... Cone-rod dystrophy Genetic Testing Registry: X-linked cone-rod dystrophy 1 Genetic Testing Registry: X-linked cone-rod dystrophy ...
    https://medlineplus.gov/genetics/condition/cone-rod-dystrophy - Genetics
  2. Retinitis pigmentosa 
    ... gov/books/NBK1417/ Citation on PubMed Hamel C. Retinitis pigmentosa. Orphanet J Rare Dis. 2006 Oct 11;1:40. doi: 10.1186/1750-1172-1-40. Citation on PubMed or Free article on PubMed Central Hartong DT, Berson EL, Dryja TP. Retinitis pigmentosa. Lancet. 2006 Nov 18;368(9549):1795-809. ...
    https://medlineplus.gov/genetics/condition/retinitis-pigmentosa - Genetics
  3. Cold-induced sweating syndrome 
    ... Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa. Am J Hum Genet. 2016 Jul 7;99(1):236-45. doi: 10.1016/j.ajhg.2016. ...
    https://medlineplus.gov/.../condition/cold-induced-sweating-syndrome - Genetics
  4. TRNT1 deficiency 
    ... EM, Slusarski DC. Hypomorphic mutations in TRNT1 cause retinitis pigmentosa with erythrocytic microcytosis. Hum Mol Genet. 2016 Jan 1;25(1):44-56. doi: 10.1093/hmg/ ...
    https://medlineplus.gov/genetics/condition/trnt1-deficiency - Genetics
  5. Usher syndrome 
    ... El-Amraoui A. Usher syndrome (sensorineural deafness and retinitis pigmentosa): pathogenesis, molecular diagnosis and therapeutic approaches. Curr Opin Neurol. 2012 Feb;25(1):42-9. doi: 10.1097/WCO.0b013e32834ef8b2. Citation ...
    https://medlineplus.gov/genetics/condition/usher-syndrome - Genetics
  6. Neuropathy, ataxia, and retinitis pigmentosa 
    ... 1):16-22. doi: 10.1136/jnnp.63.1.16. Citation on PubMed or Free article on PubMed Central
    https://medlineplus.gov/...europathy-ataxia-and-retinitis-pigmentosa - Genetics
  7. Pantothenate kinase-associated neurodegeneration 
    ... psychiatric problems.A condition called HARP (hypoprebetalipoproteinemia, acanthocytosis, retinitis ... worldwide. Mutations in ...
    https://medlineplus.gov/...enate-kinase-associated-neurodegeneration - 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 
    ... Europe, Bardet-Biedl syndrome has a prevalence of 1 in 140,000 to 1 in 160,000 newborns. The condition is more ... coast of Canada), where it affects an estimated 1 in 17,000 newborns. It also occurs more ...
    https://medlineplus.gov/genetics/condition/bardet-biedl-syndrome - Genetics
  10. Refsum disease 
    ... disease is caused by an eye disorder called retinitis pigmentosa. This disorder affects the retina, the light-sensitive ... the retina gradually deteriorate. The first sign of retinitis pigmentosa is usually a loss of night vision, which ...
    https://medlineplus.gov/genetics/condition/refsum-disease - Genetics
previous · 1 · 2 · next