ORPHA:231413
Variant of Guillain-Barré syndrome
Synonyms: Variant of GBS
- Type
- Category
- Group
- Group of disorders
- Inheritance
- Multigenic/multifactorial, Not applicable
- Age of onset
- All ages
- 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 | Variant of Guillain-Barré syndrome | Variant of GBS |
| fr | Variant du syndrome de Guillain-Barré | Variant du SGB |
| de | Guillain-Barré-Syndrom, Variante | GBS, Variante |
| es | Variante del síndrome de Guillain-Barré | Variante del GBS |
| it | Variante della sindrome di Guillain-Barré | Variante di GBS |
| nl | Variant van syndroom van Guillain-Barré | Variant van GBS |
| pt | Variante do síndrome de Guillain-Barré | |
| pl | Wariant zespołu Guillaina i Barrégo | Wariant GBS |
| cs | Varianta Guillainova-Barrého syndromu | Varianta GBS · Varianta Guillain-Barrého syndromu |
| uk | Варіант синдрому Гійєна-Барре | Варіант GBS |
| zh | 吉兰-巴雷综合征变体 | GBS变体 |
| tr | Guillain-Barrè sendromunun bir çeşidi | GBS varyantı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 16493 | E | validated | |
| UMLS | C5679837 | 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:2103Guillain-Barré syndrome
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/231413
- This record as JSON: /data/d/231413.json