Medical Subject Headings

Last uploaded: November 5, 2019
Preferred Name

Polyradiculoneuropathy, Chronic Inflammatory Demyelinating

Synonyms

Polyradiculopathies, Chronic Inflammatory

Definitions

A slowly progressive autoimmune demyelinating disease of peripheral nerves and nerve roots. Clinical manifestations include weakness and sensory loss in the extremities and enlargement of peripheral nerves. The course may be relapsing-remitting or demonstrate a step-wise progression. Protein is usually elevated in the spinal fluid and cranial nerves are typically spared. GUILLAIN-BARRE SYNDROME features a relatively rapid progression of disease which distinguishes it from this condition. (Adams et al., Principles of Neurology, 6th ed, p1337)

ID

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

altLabel

Polyradiculopathies, Chronic Inflammatory

Chronic Inflammatory Polyradiculoneuropathy

Chronic Inflammatory Polyradiculoneuropathies

CIDP

Polyradiculopathy, Chronic Inflammatory

Chronic Inflammatory Demyelinating Polyradiculoneuropathy

Polyneuropathy, Inflammatory Demyelinating, Chronic

Polyradiculoneuropathy, Chronic Inflammatory

Inflammatory Polyradiculopathies, Chronic

Chronic Inflammatory Polyradiculopathy

Polyradiculoneuropathies, Chronic Inflammatory

Inflammatory Polyradiculopathy, Chronic

Chronic Inflammatory Polyradiculopathies

AN

do not confuse X ref CHRONIC INFLAMMATORY POLYRADICULONEUROPATHY with POLYRADICULONEUROPATHY, ACUTE INFLAMMATORY see GUILLAIN-BARRE SYNDROME

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

C0393819

DC

1

definition

A slowly progressive autoimmune demyelinating disease of peripheral nerves and nerve roots. Clinical manifestations include weakness and sensory loss in the extremities and enlargement of peripheral nerves. The course may be relapsing-remitting or demonstrate a step-wise progression. Protein is usually elevated in the spinal fluid and cranial nerves are typically spared. GUILLAIN-BARRE SYNDROME features a relatively rapid progression of disease which distinguishes it from this condition. (Adams et al., Principles of Neurology, 6th ed, p1337)

DX

20000101

HN

2000

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/D000077684

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

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

Machine permutation

2000

MDA

19991105

MMR

20120703

MN

C20.111.258.750.800

C10.114.750.175

C10.314.750.700

C10.668.829.800.750.600

notation

D020277

prefLabel

Polyradiculoneuropathy, Chronic Inflammatory Demyelinating

TERMUI

T368457

T368458

T368461

T368460

T812350

T358266

T368459

TH

NLM (2000)

OMIM (2013)

tui

T047

subClassOf

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

Delete Subject Author Type Created
No notes to display
Create New Mapping

Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/OMIM/139393 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/ICD10CM/G61.81 International Classification of Diseases, Version 10 - Clinical Modification CUI