ORPHA:206970
Myotonic syndrome
- 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 | Myotonic syndrome | |
| fr | Syndrome myotonique | |
| de | Myotones Syndrom | |
| es | Síndrome miotónico | |
| it | Sindrome miotonica | |
| nl | Myotonisch syndroom | |
| pt | Síndrome miotónico | |
| pl | Zespół miotoniczny | |
| cs | Myotonický syndrom | |
| uk | Міотонічний синдром | |
| zh | 强直性综合征 | |
| tr | Miyotonik sendrom |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0016120 | E | validated | |
| MONDO | 16120 | E | validated | |
| MeSH | D020967 | E | validated | |
| UMLS | C5680798 | E | validated | |
| MedDRA | 10028658 | 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:206634Genetic skeletal muscle disease
rare genetic diseases; 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/206970
- This record as JSON: /data/d/206970.json