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loading...| Preferred Name |
Color Vision Defects [Disease/Finding] |
|
| Synonyms |
Color Vision Defects |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000000816 |
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| altLabel |
Color Vision Defects Color Vision Deficiency |
|
| cui |
C0009398 |
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| MESH DEFINITION |
Defects of color vision are mainly hereditary traits but can be secondary to acquired or developmental abnormalities in the CONES (RETINA). Severity of hereditary defects of color vision depends on the degree of mutation of the ROD OPSINS genes (on X CHROMOSOME and CHROMOSOME 3) that code the photopigments for red, green and blue. |
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| MESH DUI |
D003117 |
|
| MeSH name |
Color Vision Defects |
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| MESH UI |
M0004826 |
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| NDFRT kind |
DISEASE_KIND |
|
| notation |
N0000000816 |
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| NUI |
N0000000816 |
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| prefLabel |
Color Vision Defects [Disease/Finding] |
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| SNOMED CID |
367469000 |
|
| tui |
T047 |
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| subClassOf |
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