ORPHA:183521
Rare genetic 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 genetic movement disorder | |
| fr | Anomalie du mouvement rare de cause génétique | |
| de | Bewegungsstörung, genetisch bedingte, seltene | |
| es | Trastorno raro del movimiento de origen genético | |
| it | Disturbo genetico raro del movimento | |
| nl | Zeldzame genetische bewegingsstoornis | |
| pt | Doença do movimento, genética, raro | |
| pl | Rzadkie zaburzenia ruchu uwarunkowane genetycznie | |
| cs | Vzácné geneticky podmíněné poruchy hybnosti | |
| uk | Рідкісне генетично обумовлене порушення руху | |
| zh | 罕见遗传性运动障碍 | |
| tr | Nadir genetik hareket bozukluğu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15957 | E | validated | |
| UMLS | C5680562 | 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:71859Rare genetic neurological disorder
rare genetic diseases
Children (8):
- ORPHA:238722Familial congenital mirror movements
- ORPHA:3197Hereditary hyperekplexia
- ORPHA:163985Hyperekplexia-epilepsy syndrome
- ORPHA:369847Intellectual disability-hyperkinetic movement-truncal ataxia syndrome
- ORPHA:307058Miscellaneous movement disorder due to genetic neurodegenerative disease
- ORPHA:496916Rare genetic hyperkinetic movement disorder
- ORPHA:307052Rare genetic parkinsonian disorder
- ORPHA:306768Rare paroxysmal movement 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/183521
- This record as JSON: /data/d/183521.json