ORPHA:206707
Bulbospinal muscular atrophy of adult
- Type
- Clinical group
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Bulbospinal muscular atrophy of adult | |
| fr | Amyotrophie bulbospinale de l'adulte | |
| de | Muskelatrophie, bulbospinale, des Erwachsenen | |
| es | Atrofia muscular bulboespinal del adulto | |
| it | Atrofia muscolare bulbospinale dell'adulto | |
| nl | Bulbospinale spieratrofie bij volwassenen | Bulbospinale musculaire atrofie bij volwassenen |
| pt | Atrofia muscular bulbo-espinhal do adulto | |
| pl | Opuszkowo-rdzeniowy zanik mięśni dorosłych | |
| cs | Bulbospinální svalová atrofie dospělých | |
| uk | Бульбоспінальна мязова атрофія у дорослих | |
| zh | 成人期延髓肌萎缩 | |
| tr | Yetişkinlerde bulbospinal kas atrofisi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 16115 | E | validated | |
| UMLS | C5680796 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:206701Bulbospinal muscular atrophy
rare genetic diseases; rare neurological diseases
Children (1):
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/206707
- This record as JSON: /data/d/206707.json