ORPHA:98685
Rare oculomotor nerve disorder
- Type
- Category
- 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 | Rare oculomotor nerve disorder | |
| fr | Maladie rare du nerf oculomoteur | |
| de | Okulomotorische Lähmung | |
| es | Parálisis oculomotora | |
| it | Paralisi oculomotoria | |
| nl | Oculomotorische paralyse | Oculomotorische verlamming |
| pt | Paralisia oculomotora | |
| pl | Porażenie okoruchowe | |
| cs | Obrny okohybných svalů | |
| uk | Рідкісне захворювання окорухового нерва | |
| zh | 罕见动眼神经症 | |
| tr | Nadir okülomotor sinir bozukluğu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 1309 | E | validated | |
| UMLS | C5681697 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:522510Rare genetic ophthalmic disorder with cranial nerve involvement
rare genetic diseases - ORPHA:519349Rare ophthalmic disorder with cranial nerve involvement
rare ophthalmic disorders
Children (1):
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/98685
- This record as JSON: /data/d/98685.json