ORPHA:98494
Acquired neuromuscular junction 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 | Acquired neuromuscular junction disease | |
| fr | Maladie acquise de la jonction neuromusculaire | |
| de | Neuromuskuläre Übertragungsstörung, erworbene | |
| es | Enfermedad de la unión neuromuscular adquirida | |
| it | Malattia acquisita delle giunzioni neuromuscolari | |
| nl | Verworven neuromusculaire junctiestoornis | Verworven neuromusculaire transmissiestoornis · Verworven stoornis van de motorische eindplaat |
| pt | Doença da junção neuromuscular adquirida | |
| pl | Nabyta choroba połączeń nerwowo-mięśniowych | |
| cs | Získané choroby nervosvalové ploténky | |
| uk | Набута хвороба нервово-мязового зєднання | |
| zh | 获得性神经肌肉接头疾病 | |
| tr | Kazanılmış kas sinir kavşağı hastalığı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681732 | 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:98491Neuromuscular junction 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/98494
- This record as JSON: /data/d/98494.json