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Eye Diseases > Retinal Diseases > Retinal Degeneration > Retinal Dystrophies > Cone-Rod Dystrophies
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Eye Diseases, Hereditary > Retinal Degeneration > Retinal Dystrophies > Cone-Rod Dystrophies
Eye Diseases > Eye Diseases, Hereditary > Retinal Degeneration > Retinal Dystrophies > Cone-Rod Dystrophies

Preferred term

Cone-Rod Dystrophies  

Type

  • Topical Descriptor

Broader concept

Entry terms

  • Cone-Rod Degeneration
  • Cone Rod Degenerations
  • Cone-Rod Degenerations
  • Cone-Rod Dystrophies, Retinal
  • Cone Rod Dystrophy
  • Cone-Rod Dystrophy
  • Cone-Rod Dystrophy, Retinal
  • Cone-Rod Retinal Dystrophies
  • Cone Rod Retinal Dystrophy
  • Cone-Rod Retinal Dystrophy
  • Retinal Cone-Rod Dystrophies
  • Retinal Cone Rod Dystrophy
  • Retinal Cone-Rod Dystrophy
  • Retinal Dystrophies, Cone-Rod
  • Retinal Dystrophy, Cone-Rod

Note

  • ROD CONE DYSTROPHIES see RETINITIS PIGMENTOSA is also available

Scope note

  • Genetically heterogeneous and sometimes syndromic (e.g., BARDET BIEDL SYNDROME; and SPINOCEREBELLAR ATAXIA TYPE 7) retinopathies with initial RETINAL CONE involvement. They are characterized by decreased VISUAL ACUITY; COLOR VISION DEFECTS; progressive loss of peripheral vision and night blindness.

History note

  • 2017; use RETINITIS PIGMENTOSA 2011-2016

In other languages

URI

http://www.yso.fi/onto/mesh/D000071700

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