ORPHA:200037
Paroxysmal dystonia
- 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Paroxysmal dystonia | |
| fr | Dystonie paroxystique | |
| de | Dystonie, paroxysmale | |
| es | Distonía paroxística | |
| it | Distonia parossistica | |
| nl | Paroxysmale dystonie | |
| pt | Distonia paroxística | |
| pl | Dystonia napadowa | |
| cs | Paroxysmální dystonie | |
| uk | Пароксизмальна дистонія | |
| zh | 发作性肌张力障碍 | |
| tr | Paroksismal distoni |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | 8A02.2 | E | specific | validated |
| MONDO | 0016058 | E | validated | |
| MONDO | 16058 | E | validated | |
| UMLS | C0393588 | 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:98203Combined dystonia
rare genetic diseases; rare neurological diseases - ORPHA:306768Rare paroxysmal movement disorder
rare genetic diseases; rare neurological diseases
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/200037
- This record as JSON: /data/d/200037.json