ORPHA:494457
Rare hyperkinetic 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 hyperkinetic movement disorder | |
| fr | Trouble du mouvement hyperkinétique rare | |
| de | Seltene Form der hyperkinetischen Bewegungsstörung | |
| es | Trastorno raro del movimiento hipercinético | |
| it | Disturbo ipercinetico raro del movimento | |
| nl | Zeldzame hyperkinetische bewegingsstoornis | |
| pt | Doença do movimento hipercinético raro | |
| pl | Rzadkie zaburzenie hiperkinetyczne ruchu | |
| cs | Vzácná hyperkinetická pohybová porucha | |
| uk | Рідкісний гіперкінетичний руховий розлад | |
| zh | 罕见多动障碍 | |
| tr | Nadir hiperkinetik hareket bozukluğu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681221 | 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:102003Rare movement disorder
rare neurological diseases
Children (8):
- ORPHA:592564GNAO1-related developmental delay-seizures-movement disorder spectrum
- ORPHA:522077Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome
- ORPHA:306765Motor stereotypies
- ORPHA:684240Neurodevelopmental disorder-spasticity-movement disorder-epileptic syndrome
- ORPHA:306715Rare choreic movement disorder
- ORPHA:68363Rare dystonia
- ORPHA:306747Rare myoclonus
- ORPHA:306712Rare tremor disorder
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/494457
- This record as JSON: /data/d/494457.json