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.
Year introduced: 2017
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Subheadings:
Tree Number(s): C11.270.152, C11.768.585.658.250, C16.320.290.152
MeSH Unique ID: D000071700
Entry Terms:
- Cone Rod Dystrophies
- Cone-Rod Dystrophy
- Cone Rod Dystrophy
- Cone-Rod Degenerations
- Cone-Rod Degeneration
- Cone Rod Degenerations
- Cone-Rod Retinal Dystrophy
- Cone-Rod Retinal Dystrophies
- Cone Rod Retinal Dystrophy
- Retinal Dystrophies, Cone-Rod
- Retinal Dystrophy, Cone-Rod
- Retinal Cone-Rod Dystrophy
- Cone-Rod Dystrophies, Retinal
- Cone-Rod Dystrophy, Retinal
- Retinal Cone-Rod Dystrophies
- Retinal Cone Rod Dystrophy
- Cone-Rod Dystrophy 2
- Cone Rod Dystrophy 2
- Rod-Cone Dystrophy
- Rod-Cone Dystrophies
- Rod Cone Dystrophies
- Rod Cone Dystrophy
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