ORPHA:206982
Muscular tumor
- 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 | Muscular tumor | |
| fr | Tumeur musculaire | |
| de | Muskeltumor | |
| es | Tumor muscular | |
| it | Tumore muscolare | |
| nl | Musculaire tumor | |
| pt | Tumor muscular | |
| pl | Guz mięśni | |
| cs | Nádor ze svalové tkáně | |
| uk | Мязова пухлина | |
| zh | 肌肉肿瘤 | |
| tr | Kas tümörü |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 16123 | E | validated | |
| MeSH | D019042 | E | validated | |
| UMLS | C0282606 | E | validated | |
| MedDRA | 10070956 | 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:206638Acquired skeletal muscle 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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/206982
- This record as JSON: /data/d/206982.json