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Results 1 - 10 of 41 for "Rod-cone" dystrophy
  1. Retinitis pigmentosa 
    ... not present in other family members. Pigmentary retinopathy Rod-cone dystrophy RP Tapetoretinal degeneration Genetic Testing Registry: Retinitis pigmentosa ...
    https://medlineplus.gov/genetics/condition/retinitis-pigmentosa - 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 
    ... 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 
    ... including a group of related eye disorders called rod-cone dystrophy. Rod-cone dystrophy has signs and symptoms similar to those of cone-rod dystrophy. However, rod-cone dystrophy is characterized by deterioration of the rods first, ...
    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. Mainzer-Saldino syndrome 
    ... individuals resembles a category of retinal disorders called rod-cone dystrophies. The most common rod-cone dystrophy is called retinitis pigmentosa, and the vision problems ...
    https://medlineplus.gov/genetics/condition/mainzer-saldino-syndrome - Genetics
  7. 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
  8. 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
  9. 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
  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
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