ORPHA:306768
Rare paroxysmal 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 paroxysmal movement disorder | |
| fr | Trouble du mouvement paroxystique rare | |
| de | Bewegungsstörung, seltene paroxysmale | |
| es | Trastorno raro del movimiento paroxístico | |
| it | Disturbo raro del movimento parossistico | |
| nl | Zeldzame paroxysmale bewegingsstoornis | |
| pt | Alterações paroxístico raras do movimento | |
| pl | Rzadkie napadowe zaburzenia ruchu | |
| cs | Vzácné paroxysmální poruchy hybnosti | |
| uk | Рідкісний пароксизмальний руховий розлад | |
| zh | 罕见阵发性运动障碍 | |
| tr | Nadir paroksismal hareket bozukluğu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 17657 | E | validated | |
| UMLS | C5681054 | 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:183521Rare genetic movement disorder
rare genetic diseases - ORPHA:102003Rare 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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/306768
- This record as JSON: /data/d/306768.json