raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:231419

Functional variant of Guillain-Barré syndrome

Synonyms: Functional 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.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enFunctional variant of Guillain-Barré syndromeFunctional variant of GBS
frVariant fonctionnel du syndrome de Guillain-BarréVariant fonctionnel du SGB
deFunktionale Variante des Guillain-Barré-Syndroms
esVariante funcional del síndrome de Guillain-BarréVariante funcional del GBS
itVariante funzionale della sindrome di Guillain-BarréVariante funzionale di GBS
nlFunctionele variant van syndroom van Guillain-BarréFunctionele variant van GBS
ptVariante funcional do síndrome de Guillain-Barré
plFunkcjonalny wariant zespołu Guillaina i BarrégoFunkcjonalny wariant GBS
csFunkční varianta Guillainova-Barrého syndromuFunkční varianta GBS · Funkční varianta Guillain-Barrého syndromu
ukФункціональний варіант синдрому Гійєна-БарреФункціональний варіант GBS
zh吉兰-巴雷综合征功能性变体GBS功能性变体
trGuillain-Barrè sendromunun fonksiyonel varyantıGBS'nin fonksiyonel varyantı
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO16495Evalidated
UMLSC5679836Evalidated

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):

Children (4):

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card