{"orpha":231413,"name":"Variant of Guillain-Barré syndrome","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":["Variant of GBS"],"definition":null,"note":"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.","url":"https://raremap.alftech.space/d/ORPHA-231413/","orphanet_url":"https://www.orpha.net/en/disease/detail/231413","names":{"fr":{"name":"Variant du syndrome de Guillain-Barré","synonyms":["Variant du SGB"]},"de":{"name":"Guillain-Barré-Syndrom, Variante","synonyms":["GBS, Variante"]},"es":{"name":"Variante del síndrome de Guillain-Barré","synonyms":["Variante del GBS"]},"it":{"name":"Variante della sindrome di Guillain-Barré","synonyms":["Variante di GBS"]},"nl":{"name":"Variant van syndroom van Guillain-Barré","synonyms":["Variant van GBS"]},"pt":{"name":"Variante do síndrome de Guillain-Barré"},"pl":{"name":"Wariant zespołu Guillaina i Barrégo","synonyms":["Wariant GBS"]},"cs":{"name":"Varianta Guillainova-Barrého syndromu","synonyms":["Varianta GBS","Varianta Guillain-Barrého syndromu"]},"uk":{"name":"Варіант синдрому Гійєна-Барре","synonyms":["Варіант GBS"]},"zh":{"name":"吉兰-巴雷综合征变体","synonyms":["GBS变体"]},"tr":{"name":"Guillain-Barrè sendromunun bir çeşidi","synonyms":["GBS varyantı"]}},"xrefs":[{"source":"MONDO","code":"16493","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5679837","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":2103,"name":"Guillain-Barré syndrome","classifications":[181]}],"children":[{"orpha":231419,"name":"Functional variant of Guillain-Barré syndrome","type":"Clinical group"},{"orpha":231416,"name":"Regional variant of Guillain-Barré syndrome","type":"Clinical group"}],"genes":[],"genes_via_subtypes":[],"inheritance":["Multigenic/multifactorial","Not applicable"],"onset":["All ages"],"prevalence":[],"phenotypes":null}