ORPHA:210566
Myoclonic dystonia 15
inactive · moved to ORPHA:36899Myoclonus-dystonia syndrome
Synonyms: DYT15 · Myoclonus-dystonia type 15
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Myoclonus-dystonia syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Myoclonic dystonia 15 | DYT15 · Myoclonus-dystonia type 15 |
| fr | Dystonie myoclonique 15 | DYT15 |
| de | Myoklonus-Dystonie 15 | DYT15 |
| es | Distonía mioclónica 15 | DYT15 |
| it | Distonia mioclonica 15 | DYT15 |
| nl | Myoclonische dystonie 15 | DYT15 |
| pt | Distonia mioclónica 15 | |
| pl | Dystonia miokloniczna 15 | DYT15 |
| cs | Myoklonická dystonie 15 | DYT15 · Myoklonická dystonie, typ 15 |
| uk | Міоклонічна дистонія 15 | DYT15 · Міоклонус-дистонія типу 15 |
| zh | 肌阵挛性肌张力障碍15型 | 肌阵挛性肌张力障碍15型 |
| tr | Miyoklonik distoni 15 | DYT15 · Miyoklonus-distoni tip 15 |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 607488 | E | validated | |
| MeSH | C538002 | E | validated | |
| UMLS | C1843786 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/210566
- This record as JSON: /data/d/210566.json