ORPHA:231416
Regional variant of Guillain-Barré syndrome
Synonyms: Regional variant of GBS
- Type
- Clinical group
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Regional variant of Guillain-Barré syndrome | Regional variant of GBS |
| fr | Variant régional du syndrome de Guillain-Barré | Variant régional du SGB |
| de | Regionale Variante des Guillain-Barré-Syndroms | |
| es | Variante regional del síndrome de Guillain-Barré | Variante regional del GBS |
| it | Variante regionale della sindrome di Guillain-Barré | Variante regionale di GBS |
| nl | Regionale variant van syndroom van Guillain-Barré | Regionale variant van GBS |
| pt | Variante regional do síndrome de Guillain-Barré | |
| pl | Regionalny wariant zespołu Guillaina i Barrégo | Regionalny wariant GBS |
| cs | Regionální varianta Guillainova-Barrého syndromu | Regionální varianta GBS · Regionální varianta Guillain-Barrého syndromu |
| uk | Регіональний варіант синдрому Гійєна-Барре | Регіональний варіант GBS |
| zh | 吉兰-巴雷综合征局部变体 | GBS局部变体 |
| tr | Guillain-Barrè sendromunun bölgesel varyantı | GBS'nin bölgesel varyantı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 16494 | E | validated | |
| UMLS | C5679835 | 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:231413Variant of Guillain-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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/231416
- This record as JSON: /data/d/231416.json