Diseases

Cone-Rod Dystrophies

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.

National Library of MedicineMedical Subject Headings2026

Structured Summary

Abstract

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.

MeSH Record

Classification

Broader headings

Related Concepts

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MeSH Record

Synonyms

22 entry terms
  • Cone-Rod Degenerations
  • Cone-Rod Dystrophy
  • Cone-Rod Retinal Dystrophy
  • Retinal Cone-Rod Dystrophy
  • Cone Rod Degenerations
  • Cone Rod Dystrophies
  • Cone Rod Dystrophy
  • Cone Rod Retinal Dystrophy
  • Cone-Rod Degeneration
  • Cone-Rod Dystrophies, Retinal
  • Cone-Rod Dystrophy, Retinal
  • Cone-Rod Retinal Dystrophies
  • Retinal Cone Rod Dystrophy
  • Retinal Cone-Rod Dystrophies
  • Retinal Dystrophies, Cone-Rod
  • Retinal Dystrophy, Cone-Rod
  • Cone-Rod Dystrophy 2
  • Rod Cone Dystrophies
  • Rod-Cone Dystrophy
  • Cone Rod Dystrophy 2
  • Rod Cone Dystrophy
  • Rod-Cone Dystrophies

MeSH Record

Aspects Covered

34 allowable subheadings

Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.

MeSH Record

Indexing Annotation

ROD CONE DYSTROPHIES see RETINITIS PIGMENTOSA is also available

MeSH Record

History Note

2017; use RETINITIS PIGMENTOSA 2011-2016

MeSH Record

Previous Indexing

  • Retinal Degeneration (1975-2016)
  • Retinitis Pigmentosa (1981-2016)

MeSH Hierarchy

Tree Numbers

  1. C11w.270.152
  2. C11w.768w.585.658.250
  3. C16w.320w.290.152

AMA Style

References

  1. National Library of Medicine. Cone-Rod Dystrophies. Medical Subject Headings (MeSH). 2026. Unique ID D000071700. http://id.nlm.nih.gov/mesh/2026/D000071700
  2. Cone-Rod Dystrophies. In: Wikidata. https://www.wikidata.org/wiki/Q18553315