ORPHA:391711
Persistent combined 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 | Persistent combined dystonia | |
| fr | Dystonie combinée persistante | |
| de | Persistierende kombinierte Dystonie | |
| es | Distonía combinada persistente | |
| it | Distonia combinata persistente | |
| nl | Persisterende gecombineerde dystonie | |
| pt | Distonia persistente combinada | |
| pl | Przetrwała dystonia złożona | |
| cs | Perzistentní kombinované dystonie | Perzistující kombinované dystonie |
| uk | Персистуюча комбінована дистонія | |
| zh | 持续性联合肌张力障碍 | |
| tr | Kalıcı kombine distoni |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 18329 | E | validated | |
| UMLS | C5681153 | 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:98203Combined dystonia
rare genetic diseases; rare neurological diseases
Children (15):
- ORPHA:370109Ataxia-telangiectasia variant
- ORPHA:352649Brain dopamine-serotonin vesicular transport disease
- ORPHA:255Dopa-responsive dystonia
- ORPHA:210571Dystonia 16
- ORPHA:589618Dystonia 28
- ORPHA:412217Dystonia-aphonia syndrome
- ORPHA:521406Dystonia-parkinsonism-hypermanganesemia syndrome
- ORPHA:508523Hyperphenylalaninemia due to DNAJC12 deficiency
- ORPHA:238455Infantile dystonia-parkinsonism
- ORPHA:364063Infantile epileptic-dyskinetic encephalopathy
- ORPHA:508093MEPAN syndrome
- ORPHA:36899Myoclonus-dystonia syndrome
- ORPHA:199351PLA2G6-related neurodegeneration, adult-onset
- ORPHA:71517Rapid-onset dystonia-parkinsonism
- ORPHA:53351X-linked dystonia-parkinsonism
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/391711
- This record as JSON: /data/d/391711.json