ORPHA:68381
Neuromuscular 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 | Neuromuscular disease | |
| fr | Maladie neuromusculaire | |
| de | Neuromuskuläre Krankheit | |
| es | Enfermedad neuromuscular | |
| it | Malattia neuromuscolare | |
| nl | Neuromusculaire ziekte | |
| pt | Doença neuromuscular | |
| pl | Choroba nerwowo-mięśniowa | |
| cs | Neuromuskulární porucha | |
| uk | Нервово-мязові захворювання | |
| zh | 神经肌肉疾病 | |
| tr | Nöromüsküler hastalık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0019056 | E | validated | |
| MONDO | 19056 | E | validated | |
| MeSH | D009468 | E | validated | |
| UMLS | C0027868 | E | validated | |
| MedDRA | 10029323 | 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:98006Rare neurologic 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/68381
- This record as JSON: /data/d/68381.json