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DeCS
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Descriptor English:
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Cone-Rod Dystrophies
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Descriptor Spanish:
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Distrofias de Conos y Bastones
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Descriptor Portuguese:
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Distrofias de Cones e Bastonetes
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Synonyms English:
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Cone Rod Degenerations
Cone Rod Dystrophies
Cone Rod Dystrophy
Cone Rod Dystrophy 2
Cone Rod Retinal Dystrophy
Cone-Rod Degeneration
Cone-Rod Degenerations
Cone-Rod Dystrophies, Retinal
Cone-Rod Dystrophy
Cone-Rod Dystrophy 2
Cone-Rod Dystrophy, Retinal
Cone-Rod Retinal Dystrophies
Cone-Rod Retinal Dystrophy
Retinal Cone Rod Dystrophy
Retinal Cone-Rod Dystrophies
Retinal Cone-Rod Dystrophy
Retinal Dystrophies, Cone-Rod
Retinal Dystrophy, Cone-Rod
Rod Cone Dystrophies
Rod Cone Dystrophy
Rod-Cone Dystrophies
Rod-Cone Dystrophy
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Tree Number:
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C11.270.152
C11.768.585.658.250
C16.320.290.152
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Definition English:
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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. |
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Indexing Annotation English:
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ROD CONE DYSTROPHIES see RETINITIS PIGMENTOSA is also available
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History Note English:
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2017; use RETINITIS PIGMENTOSA 2011-2016
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Allowable Qualifiers English:
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Record Number:
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56390
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Unique Identifier:
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D000071700
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Occurrence in VHL:
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Similar:
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DeCS
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