Concept information
Término preferido
Cone-Rod Dystrophies
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Tipo
-
mesh:Descriptor
Definición
- 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.
Concepto genérico
Etiquetas alternativas
- Cone-Rod Degenerations
- Cone-Rod Dystrophy
- Cone-Rod Retinal Dystrophy
- Retinal Cone-Rod Dystrophy
En otras lenguas
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francés
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Dégénérescences des cônes et des bâtonnets
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Dystrophie des cônes et des batonnets
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Dystrophies cônes-batonnets
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Dystrophies rétiniennes mixtes
URI
http://data.loterre.fr/ark:/67375/JVR-VBKVTHQB-N
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