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 38 for "Cone-rod" dystrophy 15
  1. RPGR gene 
    ... parts of the body. COD1 CORDX1 CRD PCDX retinitis pigmentosa 15 retinitis pigmentosa 3 GTPase regulator RP15 RP3 RPGR_HUMAN X- ... Bamiou DE, Hardcastle AJ. RPGR mutation associated with retinitis pigmentosa, ... J Med Genet. 2003 Aug;40(8):609-15. doi: 10.1136/jmg.40.8.609. No ...
    https://medlineplus.gov/genetics/gene/rpgr - Genetics
  2. Cone-rod dystrophy 
    ... Registry: Cone-rod dystrophy 13 Genetic Testing Registry: Cone-rod dystrophy 15 Genetic Testing Registry: Cone-rod dystrophy 16 Genetic Testing Registry: Cone-rod dystrophy 17 ...
    https://medlineplus.gov/genetics/condition/cone-rod-dystrophy - Genetics
  3. Retinitis Pigmentosa (Foundation Fighting Blindness)  
    Retinal Disorders/Specifics ... Retinal Disorders ... Usher Syndrome/Learn More ... Usher Syndrome ... Foundation Fighting Blindness ... What is Retinitis Pigmentosa? Learn about ...
    https://www.fightingblindness.org/diseases/retinitis-pigmentosa - External Health Links
  4. USH2A gene 
    ... common cause of the autosomal recessive form of retinitis pigmentosa, accounting for 10 to 15 percent of all cases. This form of the disorder is described as nonsyndromic, which means that it is not associated with ... pigmentosa change single protein building blocks (amino acids) in ...
    https://medlineplus.gov/genetics/gene/ush2a - Genetics
  5. RP2 gene 
    ... in the human retina of the X-linked retinitis pigmentosa protein RP2, its homologue cofactor C and the RP2 interacting protein Arl3. Hum Mol Genet. 2002 Nov 15;11(24):3065-74. doi: 10.1093/hmg/ ...
    https://medlineplus.gov/genetics/gene/rp2 - Genetics
  6. Mainzer-Saldino syndrome 
    ... of cone-shaped epiphysis, renal disease in childhood, retinitis pigmentosa and abnormality of the proximal femur. Am J Med Genet A. 2007 Oct 15;143A(20):2444-7. doi: 10.1002/ajmg. ...
    https://medlineplus.gov/genetics/condition/mainzer-saldino-syndrome - Genetics
  7. Retinitis pigmentosa 
    ... in this gene are responsible for 10 to 15 percent of all cases of autosomal recessive retinitis pigmentosa. Changes in at least six genes are thought ...
    https://medlineplus.gov/genetics/condition/retinitis-pigmentosa - Genetics
  8. Choroideremia (Foundation Fighting Blindness)  
    Retinal Disorders/Specifics ... Retinal Disorders ... Eye Diseases/Specifics ... Eye Diseases ... Foundation Fighting Blindness ... What is Choroideremia? Learn about the signs ...
    https://www.fightingblindness.org/diseases/choroideremia - External Health Links
  9. Ataxia with vitamin E deficiency 
    ... this condition have developed an eye disorder called retinitis pigmentosa that causes vision loss. Most people who have ataxia with vitamin E deficiency start to experience problems with movement between the ages of 5 and 15 years. The movement problems tend to worsen with ...
    https://medlineplus.gov/.../ataxia-with-vitamin-e-deficiency - Genetics
  10. Vitelliform macular dystrophy 
    ... retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or ... and other maculopathies. Hum Mutat. 2000;15(4):301-8. doi: 10.1002/(SICI)1098- ...
    https://medlineplus.gov/.../condition/vitelliform-macular-dystrophy - Genetics
previous · 1 · 2 · 3 · 4 · next