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loading...| Preferred Name |
Cone-Rod Dystrophies [Disease/Finding] |
|
| Synonyms |
Cone-Rod Dystrophies Cone-Rod Dystrophy Cone-Rod Retinal Dystrophy Retinal Cone-Rod Dystrophy Cone-Rod Degenerations |
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| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000192930 |
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| altLabel |
Cone-Rod Dystrophies Cone-Rod Dystrophy Cone-Rod Retinal Dystrophy Retinal Cone-Rod Dystrophy Cone-Rod Degenerations |
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| cui |
C4085590 |
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| MESH DEFINITION |
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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| MESH DUI |
D000071700 |
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| MeSH name |
Cone-Rod Dystrophies |
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| MESH UI |
M000615345 |
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| NDFRT kind |
DISEASE_KIND |
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| notation |
N0000192930 |
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| NUI |
N0000192930 |
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| prefLabel |
Cone-Rod Dystrophies [Disease/Finding] |
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| tui |
T047 |
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| subClassOf |
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