ORPHA:98472
Skeletal muscle disease
- 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 | Skeletal muscle disease | |
| fr | Maladie du muscle squelettique | |
| de | Skelettmuskel-Krankheit | |
| es | Enfermedad del músculo esquelético | |
| it | Malattia dei muscoli scheletrici | |
| nl | Skeletspierziekte | |
| pt | Doença muscular esquelética | |
| pl | Choroba mięśni szkieletowych | |
| cs | Choroby kosterních svalů | |
| uk | Захворювання скелетних мязів | |
| zh | 骨骼肌疾病 | |
| tr | İskelet kası hastalığı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0020120 | E | validated | |
| MeSH | D009135 | E | validated | |
| MedDRA | 10028641 | 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:68381Neuromuscular disease
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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/98472
- This record as JSON: /data/d/98472.json