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Searched for "Retinal Degeneration".

29 results found on Genetics Home Reference.

Showing results 1 to 20.
  • spastic paraplegia type 15 condition summary
    Found in name or synonym: spastic paraplegia and retinal degeneration
    Related genes:
  • retinitis pigmentosa condition summary
    Found: ...copy of the gene develop retinal degeneration and associated vision loss. In...
    Related genes:
  • age-related macular degeneration condition summary
    Related classification: Retinal Degeneration
    Related genes:
  • Alström syndrome condition summary
    Related classification: Retinal Degeneration
    Related genes:
  • Bietti crystalline dystrophy condition summary
    Related classification: Retinal Degeneration
    Related genes:
  • juvenile Batten disease condition summary
    Related term: retinal degeneration
    Related genes:
  • Kearns-Sayre syndrome condition summary
    Related classification: Retinal Degeneration
  • Stargardt macular degeneration condition summary
    Related classification: Retinal Degeneration
    Related genes:
  • Usher syndrome condition summary
    Related classification: Retinal Degeneration
  • vitelliform macular dystrophy condition summary
    Related classification: Retinal Degeneration
    Related genes:
  • X-linked juvenile retinoschisis condition summary
    Related classification: Retinal Degeneration
    Related genes:
  • Mainzer-Saldino syndrome condition summary
    Found: ...Mainzer-Saldino syndrome, the retinal degeneration begins in childhood, but some vision...
    Related genes:
  • NPHP1 gene summary
    Official name: nephronophthisis 1 (juvenile)
    Found: ...and breakdown of the retina (retinal degeneration). Joubert syndrome is a multisystem...
  • nephronophthisis condition summary
    Found: ...tissue at the back of the eye (retinal degeneration); Joubert syndrome affects many...
    Related genes:
  • C1QTNF5 gene information
    Official name: C1q and tumor necrosis factor related protein 5
    Found: Late-onset retinal degeneration (LORD): Autosomal dominant disorder...
  • ACO2 gene information
    Official name: aconitase 2, mitochondrial
    Found: Infantile cerebellar-retinal degeneration (ICRD): A severe autosomal recessive...
  • RBP4 gene information
    Official name: retinol binding protein 4, plasma
    Found: ...A disease characterized by retinal degeneration, ocular colobomas involving both...
  • BBS7 gene information
    Official name: Bardet-Biedl syndrome 7
    Found: ...clinical features include retinal degeneration, renal cystic disease, skeletal...
  • ATXN7 gene information
    Official name: ataxin 7
    Found: ...which always presents with retinal degeneration (SCA7), and ADCAIII often referred...
  • PRCD gene information
    Official name: progressive rod-cone degeneration
    Found: ...cause of autosomal recessive retinal degeneration in both humans and dogs. Alternatively...
 
Published: November 17, 2014