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 46 for "Cone-rod" dystrophy 2
  1. 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 ... the vision loss results from a condition called retinitis pigmentosa. This eye disease causes the light-sensing cells ...
    https://medlineplus.gov/...europathy-ataxia-and-retinitis-pigmentosa - Genetics
  2. Retinitis pigmentosa 
    Retinitis pigmentosa is a group of related eye disorders that cause progressive vision loss. These disorders affect the retina, which is the layer of light-sensitive ...
    https://medlineplus.gov/genetics/condition/retinitis-pigmentosa - Genetics
  3. RPGR gene 
    ... found to cause the X-linked form of retinitis pigmentosa. This condition primarily affects males, causing night blindness ... 70 percent of all cases of X-linked retinitis pigmentosa.Most of the mutations responsible for X-linked ...
    https://medlineplus.gov/genetics/gene/rpgr - Genetics
  4. Cone-rod dystrophy 
    ... Registry: Cone-rod dystrophy 19 Genetic Testing Registry: Cone-rod dystrophy 2 Genetic Testing Registry: Cone-rod dystrophy 20 Genetic ... National Organization for Rare Disorders (NORD) ClinicalTrials.gov CONE-ROD DYSTROPHY 2; CORD2 CONE-ROD DYSTROPHY 1; CORD1 CONE-ROD ...
    https://medlineplus.gov/genetics/condition/cone-rod-dystrophy - Genetics
  5. Usher syndrome 
    ... vision is caused by an eye disease called retinitis pigmentosa (RP), which affects the layer of light-sensitive ... of the eye (cataracts). However, many people with retinitis pigmentosa retain some central vision throughout their lives.Researchers ...
    https://medlineplus.gov/genetics/condition/usher-syndrome - Genetics
  6. Bardet-Biedl syndrome 
    Bardet-Biedl syndrome is a disorder that affects many parts of the body. The signs and symptoms of this condition vary among affected individuals, even among ...
    https://medlineplus.gov/genetics/condition/bardet-biedl-syndrome - Genetics
  7. RHO gene 
    ... light that remains stable (stationary) over time. Unlike retinitis pigmentosa (described below), autosomal dominant congenital stationary night blindness ...
    https://medlineplus.gov/genetics/gene/rho - Genetics
  8. RP2 gene 
    ... in people with the X-linked form of retinitis pigmentosa. This condition primarily affects males, causing night blindness ... 15 percent of all cases of X-linked retinitis pigmentosa.Most mutations in the RP2 gene lead to ...
    https://medlineplus.gov/genetics/gene/rp2 - Genetics
  9. PRPH2 gene 
    ... in the PRPH2 gene can cause autosomal dominant retinitis pigmentosa, an eye disease that first disrupts night vision ... other retinal disorders caused by PRPH2 gene mutations, retinitis pigmentosa involves a slow degeneration of photoreceptor cells, leading ...
    https://medlineplus.gov/genetics/gene/prph2 - Genetics
  10. USH2A gene 
    ... the USH2A gene have been reported to cause retinitis pigmentosa, a vision disorder that causes the light-sensing ... common cause of the autosomal recessive form of retinitis pigmentosa, accounting for 10 to 15 percent of all ...
    https://medlineplus.gov/genetics/gene/ush2a - Genetics
previous · 1 · 2 · 3 · 4 · 5 · next