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Concept information

Preferred term

Optic Atrophy, Autosomal Dominant  

Type

  • mesh:Descriptor

Definition

  • Dominant optic atrophy is a hereditary optic neuropathy causing decreased visual acuity, color vision deficits, a centrocecal scotoma, and optic nerve pallor (Hum. Genet. 1998; 102: 79-86). Mutations leading to this condition have been mapped to the OPA1 gene at chromosome 3q28-q29. OPA1 codes for a dynamin-related GTPase that localizes to mitochondria.

Entry terms

  • Autosomal Dominant Optic Atrophy
  • Autosomal Dominant Optic Atrophy Kjer Type
  • Dominant Optic Atrophy
  • Kjer's Optic Atrophy
  • Kjer Type Optic Atrophy
  • Kjer-Type Optic Atrophy
  • Optic Atrophy 1
  • Optic Atrophy, Hereditary, Autosomal Dominant
  • Optic Atrophy, Juvenile
  • Optic Atrophy, Kjer Type
  • Optic Atrophy Type 1

In other languages

  • French

  • Atrophie du nerf optique autosomique dominante
  • Atrophie optique dominante
  • Atrophie optique dominante de Kjer
  • Atrophie optique dominante de type 1
  • Atrophie optique dominante de type I
  • Maladie de Kjer

URI

http://data.loterre.fr/ark:/67375/JVR-TRH09QKJ-0

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RDF/XML TURTLE JSON-LD Created 7/25/01, last modified 7/8/13