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Eye Diseases > Uveal Diseases > Choroid Diseases > Gyrate Atrophy
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Eye Diseases, Hereditary > Gyrate Atrophy
Eye Diseases > Eye Diseases, Hereditary > Gyrate Atrophy

Preferred term

Gyrate Atrophy  

Type

  • Topical Descriptor

Broader concept

Entry terms

  • Gyrate Atrophy of Choroid and Retina
  • Gyrate Atrophy of the Choroid and Retina
  • Hyperornithinemia with Gyrate Atrophy of Choroid and Retina
  • Ornithinemia with Gyrate Atrophy

Note

  • a hered eye dis; /congen permitted: read MeSH definition

Scope note

  • Progressive, autosomal recessive, diffuse atrophy of the choroid, pigment epithelium, and sensory retina that begins in childhood.

History note

  • 90

In other languages

URI

http://www.yso.fi/onto/mesh/D015799

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