ORPHA:306712
Rare tremor 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 tremor disorder | |
| fr | Tremblement rare | |
| de | Tremorkrankheit, seltene | |
| es | Temblor raro | |
| it | Tremore raro | |
| nl | Zeldzame tremorstoornis | |
| pt | Alterações raras do tremor | |
| pl | Rzadkie zaburzenia z drżeniem | |
| cs | Vzácné třesové poruchy | |
| uk | Рідкісний тремор | |
| zh | 罕见震颤症 | |
| tr | Nadir titreme bozukluğu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 17644 | E | validated | |
| UMLS | C5681066 | 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
Children (7):
- ORPHA:93256Fragile X-associated tremor/ataxia syndrome
- ORPHA:53372Hereditary geniospasm
- ORPHA:238606Primary orthostatic tremor
- ORPHA:457212Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome
- ORPHA:66633Sensorineural hearing loss-early graying-essential tremor syndrome
- ORPHA:3350Tremor-nystagmus-duodenal ulcer syndrome
- ORPHA:905Wilson disease
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/306712
- This record as JSON: /data/d/306712.json