Chronic inflammatory demyelinating polyradiculoneuropathy

disorder

SNOMED 128209004CUI C0393819

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Absent tendon reflexes

Very frequent (80-99%)HP:0001284

Decreased nerve conduction velocity

Very frequent (80-99%)HP:0000762

Fatiguable weakness of proximal limb muscles

Very frequent (80-99%)HP:0030200

Motor conduction block

Very frequent (80-99%)HP:0012078

Nerve conduction abnormalities

Very frequent (80-99%)HP:0040129

Paresthesia

Very frequent (80-99%)HP:0003401

Peripheral demyelination

Very frequent (80-99%)HP:0011096

Peripheral neuropathy

Very frequent (80-99%)HP:0009830

Segmental peripheral demyelination/remyelination

Very frequent (80-99%)HP:0003481

Sensory ataxia

Very frequent (80-99%)HP:0010871

Sensory impairment

Very frequent (80-99%)HP:0003474

Unsteady walk

Very frequent (80-99%)HP:0002317

Anti-contactin-1 antibody positivity

Frequent (30-79%)HP:0034137

Anti-contactin-associated protein 1 antibody positivity

Frequent (30-79%)HP:0034138

Anti-neurofascin 186 antibody positivity

Frequent (30-79%)HP:0034136

Anti-NF155 antibody positivity

Frequent (30-79%)HP:0034135

Difficulty walking up stairs

Frequent (30-79%)HP:0003551

Falls

Frequent (30-79%)HP:0002527

Gait disturbance

Frequent (30-79%)HP:0001288

Hand muscle weakness

Frequent (30-79%)HP:0030237

Spontaneous pain sensation

Occasional (5-29%)HP:0010833

Acute demyelinating polyneuropathy

HP:0007131

Related Conditions

Chronic inflammatory demyelinating polyradiculoneuropathy with central nervous system demyelination(child)

Chronic ataxic neuropathy, ophthalmoplegia, monoclonal immunoglobulin M protein, cold agglutinin and disialosyl antibody syndrome(child)

Brachial variant of chronic immune demyelinating polyradiculoneuropathy(child)

Chronic inflammatory demyelinating disease of peripheral nervous system and central nervous system(child)

Demyelinating polyneuropathy(parent)

Chronic nervous system disease(parent)

Polyradiculoneuropathy(parent)

Polyneuritis(parent)

Quick Facts

SNOMED CT: 128209004
UMLS CUI: C0393819
Fully Specified Name: Chronic inflammatory demyelinating polyradiculoneuropathy (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 22

Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.