ORPHA:98486
Metabolic myopathy
- 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 | Metabolic myopathy | |
| fr | Myopathie d'origine métabolique | |
| de | Myopathie, metabolische | |
| es | Miopatía metabólica | |
| it | Malattia metabolica del muscolo | |
| nl | Metabole myopathie | |
| pt | Miopatia metabólica | |
| pl | Miopatia metaboliczna | |
| cs | Metabolická myopatie | |
| uk | Метаболічна міопатія | |
| zh | 代谢性肌病 | |
| tr | Metabolik miyopati |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0020123 | E | validated | |
| UMLS | C0270984 | E | validated | |
| MedDRA | 10068836 | 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:206656Non-dystrophic myopathy
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/98486
- This record as JSON: /data/d/98486.json