ORPHA:68363
Rare dystonia
Synonyms: Rare dystonic 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare dystonia | Rare dystonic disorder |
| fr | Dystonie rare | |
| de | Dystonie, seltene | |
| es | Distonía rara | |
| it | Malattia distonica | |
| nl | Zeldzame dystonie | Zeldzame dystonische stoornis |
| pt | Distonia rara | |
| pl | Rzadkie rodzaje dystonii | Rzadkie zaburzenia dystoniczne |
| cs | Vzácná dystonie | Vzácná dystonická porucha |
| uk | Рідкісна дистонія | Рідкісний дистонічний розлад |
| zh | 罕见肌张力障碍 | 罕见肌张力障碍 |
| tr | Nadir distoni | Nadir distonik bozukluk |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 19049 | E | validated | |
| UMLS | C5680168 | 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 (1):
- ORPHA:494457Rare hyperkinetic movement disorder
rare neurological diseases
Codes that Orphanet moved or referred to this one:
- ORPHA:71516OBSOLETE: Mixed dystonia 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/68363
- This record as JSON: /data/d/68363.json