Medical Subject Headings

Last uploaded: November 5, 2019
Preferred Name

Guillain-Barre Syndrome

Synonyms

Infectious Polyneuritis, Acute

Definitions

An acute inflammatory autoimmune neuritis caused by T cell- mediated cellular immune response directed towards peripheral myelin. Demyelination occurs in peripheral nerves and nerve roots. The process is often preceded by a viral or bacterial infection, surgery, immunization, lymphoma, or exposure to toxins. Common clinical manifestations include progressive weakness, loss of sensation, and loss of deep tendon reflexes. Weakness of respiratory muscles and autonomic dysfunction may occur. (From Adams et al., Principles of Neurology, 6th ed, pp1312-1314)

ID

http://purl.bioontology.org/ontology/MESH/D020275

altLabel

Infectious Polyneuritis, Acute

Syndromes, Familial Guillain-Barre

Landry Guillain Barre Syndrome

Syndromes, Guillain-Barré

Autoimmune Neuropathy, Acute

Acute Autoimmune Neuropathy

Syndrome, Guillaine-Barre

Syndrome, Guillain-Barre

Guillaine Barre Syndrome

Acute Inflammatory Polyradiculoneuropathy

Familial Guillain-Barre Syndrome

Landry-Guillain-Barre Syndrome

Syndrome, Familial Guillain-Barre

Guillain Barre Syndrome, Familial

Inflammatory Polyneuropathy Acute

Acute Inflammatory Demyelinating Polyradiculoneuropathy

Acute Infectious Polyneuritis

Guillain-Barre Syndromes, Familial

Polyradiculoneuropathy, Acute Inflammatory

Inflammatory Demyelinating Polyradiculoneuropathy, Acute

Polyneuropathy, Acute Inflammatory

Syndrome, Guillain-Barré

Polyneuropathy Acute, Inflammatory

Inflammatory Polyneuropathies, Acute

Acute Inflammatory Polyneuropathy

Acute Inflammatory Polyradiculoneuropathies

Polyneuropathies, Acute Inflammatory

Polyneuropathy, Inflammatory Demyelinating, Acute

Polyradiculoneuropathies, Acute Inflammatory

Guillain Barre Syndrome

Neuropathies, Acute Autoimmune

Guillain-Barre Syndrome, Familial

Demyelinating Polyradiculoneuropathy, Acute Inflammatory

Guillain Barré Syndrome

Autoimmune Neuropathies, Acute

Inflammatory Polyneuropathy, Acute

Guillain-Barré Syndrome

Polyneuritis, Acute Infectious

Neuropathy, Acute Autoimmune

Syndrome, Landry-Guillain-Barre

Inflammatory Polyradiculoneuropathies, Acute

Acute Autoimmune Neuropathies

Familial Guillain-Barre Syndromes

Acute Inflammatory Demyelinating Polyneuropathy

Guillain-Barré Syndromes

Guillaine-Barre Syndrome

Polyradiculoneuropathy, Acute Inflammatory Demyelinating

Acute Inflammatory Polyneuropathies

AN

do not confuse entry term POLYRADICULONEUROPATHY, ACUTE INFLAMMATORY with POLYRADICULONEUROPATHY, CHRONIC INFLAMMATORY see POLYRADICULONEUROPATHY, CHRONIC INFLAMMATORY DEMYELINATING

AQL

BL CF CI CL CN CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI

cui

C3542501

C0018378

C4083008

C4551910

DC

1

definition

An acute inflammatory autoimmune neuritis caused by T cell- mediated cellular immune response directed towards peripheral myelin. Demyelination occurs in peripheral nerves and nerve roots. The process is often preceded by a viral or bacterial infection, surgery, immunization, lymphoma, or exposure to toxins. Common clinical manifestations include progressive weakness, loss of sensation, and loss of deep tendon reflexes. Weakness of respiratory muscles and autonomic dysfunction may occur. (From Adams et al., Principles of Neurology, 6th ed, pp1312-1314)

DX

20000101

HN

2000; use POLYRADICULONEUROPATHY 1979-1999

Inverse of AQ

http://purl.bioontology.org/ontology/MESH/Q000401

http://purl.bioontology.org/ontology/MESH/Q000150

http://purl.bioontology.org/ontology/MESH/Q000188

http://purl.bioontology.org/ontology/MESH/Q000517

http://purl.bioontology.org/ontology/MESH/Q000201

http://purl.bioontology.org/ontology/MESH/Q000145

http://purl.bioontology.org/ontology/MESH/Q000503

http://purl.bioontology.org/ontology/MESH/Q000453

http://purl.bioontology.org/ontology/MESH/Q000208

http://purl.bioontology.org/ontology/MESH/Q000134

http://purl.bioontology.org/ontology/MESH/Q000821

http://purl.bioontology.org/ontology/MESH/Q000382

http://purl.bioontology.org/ontology/MESH/Q000601

http://purl.bioontology.org/ontology/MESH/Q000235

http://purl.bioontology.org/ontology/MESH/Q000523

http://purl.bioontology.org/ontology/MESH/Q000276

http://purl.bioontology.org/ontology/MESH/Q000191

http://purl.bioontology.org/ontology/MESH/Q000652

http://purl.bioontology.org/ontology/MESH/Q000662

http://purl.bioontology.org/ontology/MESH/Q000151

http://purl.bioontology.org/ontology/MESH/Q000628

http://purl.bioontology.org/ontology/MESH/Q000196

http://purl.bioontology.org/ontology/MESH/Q000534

http://purl.bioontology.org/ontology/MESH/Q000266

http://purl.bioontology.org/ontology/MESH/Q000532

http://purl.bioontology.org/ontology/MESH/Q000139

http://purl.bioontology.org/ontology/MESH/Q000378

http://purl.bioontology.org/ontology/MESH/Q000175

http://purl.bioontology.org/ontology/MESH/Q000000981

http://purl.bioontology.org/ontology/MESH/Q000097

http://purl.bioontology.org/ontology/MESH/Q000473

http://purl.bioontology.org/ontology/MESH/Q000451

http://purl.bioontology.org/ontology/MESH/Q000209

http://purl.bioontology.org/ontology/MESH/Q000178

http://purl.bioontology.org/ontology/MESH/Q000469

Inverse of SIB

http://purl.bioontology.org/ontology/MESH/D011843

http://purl.bioontology.org/ontology/MESH/D059348

http://purl.bioontology.org/ontology/MESH/D053421

http://purl.bioontology.org/ontology/MESH/D020386

http://purl.bioontology.org/ontology/MESH/D000077684

http://purl.bioontology.org/ontology/MESH/D000170

http://purl.bioontology.org/ontology/MESH/D000699

http://purl.bioontology.org/ontology/MESH/D056768

http://purl.bioontology.org/ontology/MESH/D017772

http://purl.bioontology.org/ontology/MESH/D020422

http://purl.bioontology.org/ontology/MESH/D009456

http://purl.bioontology.org/ontology/MESH/D011128

http://purl.bioontology.org/ontology/MESH/D020918

http://purl.bioontology.org/ontology/MESH/D010524

http://purl.bioontology.org/ontology/MESH/D009408

http://purl.bioontology.org/ontology/MESH/D052958

http://purl.bioontology.org/ontology/MESH/D009443

http://purl.bioontology.org/ontology/MESH/D020277

http://purl.bioontology.org/ontology/MESH/D003929

http://purl.bioontology.org/ontology/MESH/D011115

http://purl.bioontology.org/ontology/MESH/D020516

http://purl.bioontology.org/ontology/MESH/D009437

http://purl.bioontology.org/ontology/MESH/D000071075

Machine permutation

2000; see POLYRADICULONEURITIS 1979-1999

MDA

19991103

MMR

20180314

MN

C10.668.829.350

C10.668.829.800.750.300

C10.314.750.450

C20.111.258.750.400

C10.114.750.100

notation

D020275

prefLabel

Guillain-Barre Syndrome

TERMUI

T032746

T368425

T368423

T841558

T368427

T804393

T752564

T368430

T368420

T368422

T368419

T804394

T368426

T368424

T368431

T368428

T841557

T368418

TH

UNK (19XX)

NLM (2000)

NLM (2010)

NLM (2014)

ORD (2010)

OMIM (2013)

GHR (2014)

tui

T047

subClassOf

http://purl.bioontology.org/ontology/MESH/D011129

http://purl.bioontology.org/ontology/MESH/D010523

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http://purl.bioontology.org/ontology/OMIM/139393 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/139393 Online Mendelian Inheritance in Man CUI
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C116345 National Cancer Institute Thesaurus LOOM
http://purl.bioontology.org/ontology/MEDLINEPLUS/C3542501 MedlinePlus Health Topics CUI
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0018378 MedlinePlus Health Topics CUI
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0018378 MedlinePlus Health Topics LOOM
http://purl.bioontology.org/ontology/ICD10CM/G61.0 International Classification of Diseases, Version 10 - Clinical Modification CUI
http://purl.bioontology.org/ontology/ICD10CM/G61.0 International Classification of Diseases, Version 10 - Clinical Modification LOOM
http://purl.obolibrary.org/obo/DOID_12842 Human Disease Ontology 123 LOOM
http://purl.bmicc.cn/ontology/ICD10CN/G61.0 International Classification of Diseases, 10th Edition, China CUI
http://purl.bioontology.org/ontology/ICD10/G61.0 International Classification of Diseases, Version 10 CUI
http://purl.bioontology.org/ontology/ICD10/G61.0 International Classification of Diseases, Version 10 LOOM