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 31 - 38 of 38 for Retinitis pigmentosa 1
  1. Mitochondrial DNA 
    ... been found in people with neuropathy, ataxia, and retinitis pigmentosa (NARP). The MT-ATP6 gene provides instructions for ...
    https://medlineplus.gov/genetics/chromosome/mitochondrial-dna - Genetics
  2. ALG6-congenital disorder of glycosylation 
    ... same direction (strabismus) and an eye disorder called retinitis pigmentosa, which causes vision loss. Females with ALG6-CDG ...
    https://medlineplus.gov/...alg6-congenital-disorder-of-glycosylation - Genetics
  3. Vitelliform macular dystrophy 
    ... retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy. Nat Genet. 1993 Mar;3( ...
    https://medlineplus.gov/.../condition/vitelliform-macular-dystrophy - Genetics
  4. Nearsightedness 
    ... congenital stationary night blindness, Stickler syndrome, Marfan syndrome, retinitis pigmentosa, cone-rod dystrophy, deafness and myopia syndrome, Knobloch ...
    https://medlineplus.gov/genetics/condition/nearsightedness - Genetics
  5. CLN11 disease 
    ... time and is due to a condition called retinitis pigmentosa, which is caused by the breakdown of the ...
    https://medlineplus.gov/genetics/condition/cln11-disease - Genetics
  6. PMM2-congenital disorder of glycosylation 
    ... Some affected individuals have an eye disorder called retinitis pigmentosa that causes vision loss. Females with PMM2-CDG ...
    https://medlineplus.gov/...pmm2-congenital-disorder-of-glycosylation - Genetics
  7. PDE6B gene 
    ... This Health Condition MedlinePlus Genetics provides information about Retinitis pigmentosa More About This Health Condition GMP-PDE beta ...
    https://medlineplus.gov/genetics/gene/pde6b - Genetics
  8. PANK2 gene 
    ... people with a condition called HARP (hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration). HARP was historically described as ...
    https://medlineplus.gov/genetics/gene/pank2 - Genetics
previous · 1 · 2 · 3 · 4 · next