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loading...| Preferred Name |
Optic Atrophies, Hereditary [Disease/Finding] |
|
| Synonyms |
Optic Atrophies, Hereditary |
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| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000003230 |
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| altLabel |
Optic Atrophies, Hereditary Hereditary Optic Atrophy Optic Atrophy, Hereditary |
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| cui |
C0029125 |
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| MESH DEFINITION |
Hereditary conditions that feature progressive visual loss in association with optic atrophy. Relatively common forms include autosomal dominant optic atrophy (OPTIC ATROPHY, AUTOSOMAL DOMINANT) and Leber hereditary optic atrophy (OPTIC ATROPHY, HEREDITARY, LEBER). |
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| MESH DUI |
D015418 |
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| MeSH name |
Optic Atrophies, Hereditary |
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| MESH UI |
M0023768 |
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| NDFRT kind |
DISEASE_KIND |
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| notation |
N0000003230 |
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| NUI |
N0000003230 |
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| prefLabel |
Optic Atrophies, Hereditary [Disease/Finding] |
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| SNOMED CID |
26360005 |
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| tui |
T047 |
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| subClassOf |
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