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loading...| Preferred Name | Optic Atrophy [Disease/Finding] | |
| Synonyms |
Optic Atrophy |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000002226 |
|
| altLabel |
Optic Atrophy |
|
| cui |
C0029124 |
|
| MESH DEFINITION |
Atrophy of the optic disk which may be congenital or acquired. This condition indicates a deficiency in the number of nerve fibers which arise in the RETINA and converge to form the OPTIC DISK; OPTIC NERVE; OPTIC CHIASM; and optic tracts. GLAUCOMA; ISCHEMIA; inflammation, a chronic elevation of intracranial pressure, toxins, optic nerve compression, and inherited conditions (see OPTIC ATROPHIES, HEREDITARY) are relatively common causes of this condition. |
|
| MESH DUI |
D009896 |
|
| MeSH name |
Optic Atrophy |
|
| MESH UI |
M0015352 |
|
| NDFRT kind |
DISEASE_KIND |
|
| notation |
N0000002226 |
|
| NUI |
N0000002226 |
|
| prefLabel |
Optic Atrophy [Disease/Finding] |
|
| SNOMED CID |
194042009 76976005 95774001 |
|
| tui |
T047 |
|
| subClassOf |
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