ORPHA:221114
Acquired peripheral 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 | Acquired peripheral movement disorder | |
| fr | Anomalie du mouvement périphérique acquise | |
| de | Bewegungsstörung, erworbene periphere | |
| es | Anomalía adquirida del movimiento periférico | |
| it | Disturbo del movimento periferico acquisito | |
| nl | Verworven perifere bewegingsstoornis | |
| pt | Doença do movimento periférica, adquirida | |
| pl | Nabyte obwodowe zaburzenie ruchowe | |
| cs | Získaná porucha periferní hybnosti | |
| uk | Набутий периферичний руховий розлад | |
| zh | 获得性外周运动障碍 | |
| tr | Edinsel periferik hareket bozukluğu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 16375 | E | validated | |
| UMLS | C5680889 | 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:182086Acquired peripheral neuropathy
rare neurological diseases
Children (2):
Codes that Orphanet moved or referred to this one:
- ORPHA:221106OBSOLETE: Isolated facial myokymia 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/221114
- This record as JSON: /data/d/221114.json