ORPHA:306715
Rare choreic 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare choreic movement disorder | |
| fr | Maladie rare avec mouvements choréiques | |
| de | Seltene Bewegungsstörung mit Chorea | |
| es | Enfermedad rara con movimientos coréicos | |
| it | Malattia rara con movimenti coreici | |
| nl | Zeldzame choreïsche bewegingsstoornis | |
| pt | Alterações raras do movimento | |
| pl | Rzadkie zaburzenia ruchu z pląsawicą | |
| cs | Vzácné poruchy hybnosti s choreou | |
| uk | Рідкісний хореїчний руховий розлад | |
| zh | 罕见舞蹈运动障碍 | |
| tr | Nadir koreik hareket bozukluğu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 17645 | E | validated | |
| UMLS | C5681065 | 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
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/306715
- This record as JSON: /data/d/306715.json