ORPHA:98687
Supranuclear eye movement 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 | Supranuclear eye movement disorder | |
| fr | Maladie oculomotrice supranucléaire | |
| de | Paralyse, okulomotorische supranukleäre | |
| es | Parálisis supranuclear oculomotora | |
| it | Paralisi oculomotoria sopranucleare | |
| nl | Supranucleaire oculomotorische paralyse | Supranucleaire oculomotorische verlamming |
| pt | Paralisia oculomotora supranuclear | |
| pl | Nadjądrowe porażenie okoruchowe | |
| cs | Supranukleární obrny okohybných svalů | |
| uk | Супрануклеарний розлад руху очей | |
| zh | 核上性眼球运动障碍 | |
| tr | Supranükleer göz hareketi bozukluğu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681698 | 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 (2):
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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/98687
- This record as JSON: /data/d/98687.json