ORPHA:306750
Primary myoclonus
- 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 | Primary myoclonus | |
| fr | Myoclonie primaire | |
| de | Myoklonie, primäre | |
| es | Mioclono primario | |
| it | Mioclonia primitiva | |
| nl | Primaire myoclonus | |
| pt | Mioclonia primária | |
| pl | Mioklonus pierwotny | |
| cs | Primární myoklonus | |
| uk | Первинний міоклонус | |
| zh | 原发性肌阵挛 | |
| tr | Primer miyoklonus |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 17651 | E | validated | |
| UMLS | C5681052 | 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:307064Rare genetic myoclonus
rare genetic diseases - ORPHA:306747Rare myoclonus
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/306750
- This record as JSON: /data/d/306750.json