ORPHA:499047
Autoimmune/inflammatory optic neuropathy
- Type
- Clinical group
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Autoimmune/inflammatory optic neuropathy | |
| fr | Neuropathie optique autoimmune ou inflammatoire | |
| de | Autoimmune/inflammatorische Optikusneuropathie | |
| es | Neuropatía óptica autoinmune/inflamatoria | |
| it | Neuropatia ottica autoimmune / infiammatoria | |
| nl | Auto-immune/inflammatoire opticusneuropathie | Auto-immune/inflammatoire optische neuropathie |
| pt | Neuropatia óptica auto-imune/inflamatória | |
| pl | Neuropatia tarczy nerwu wzrokowego autoimmunologiczna/zapalna | |
| cs | Autoimunitní/inflamatorní neuropatie optiku | |
| uk | Аутоімунна/запальна нейропатія зорового нерва | |
| zh | 自身免疫/炎症性视神经病变 | |
| tr | Otoimmün/inflamatuar optik nöropati |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0044685 | E | validated | |
| UMLS | C5681239 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:519351Rare optic nerve disorder
rare ophthalmic disorders
Codes that Orphanet moved or referred to this one:
- ORPHA:519335OBSOLETE: Inflammatory/autoimmune optic neuropathy referred to · inactive
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/499047
- This record as JSON: /data/d/499047.json