Chronic infantile neurological, cutaneous and articular syndrome

disorder

SNOMED 239826001CUI C0409818

Overview

Chronic infantile neurological, cutaneous and articular syndrome is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Signs & Symptoms

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

Hepatosplenomegaly

Always present (100%)HP:0001433

Skin rash

Always present (100%)HP:0000988

Abnormality of granulocytes

Very frequent (80-99%)HP:0001911

Abnormality of neutrophils

Very frequent (80-99%)HP:0001874

Arthralgias

Very frequent (80-99%)HP:0002829

Brachydactyly

Very frequent (80-99%)HP:0001156

Deafness

Very frequent (80-99%)HP:0000365

Elevated C-reactive protein level

Very frequent (80-99%)HP:0011227

Elevated sedimentation rate

Very frequent (80-99%)HP:0003565

Hives

Very frequent (80-99%)HP:0001025

Inflammatory abnormality of the eye

Very frequent (80-99%)HP:0100533

Intermittent fever

Very frequent (80-99%)HP:0001954

Joint inflammation

Very frequent (80-99%)HP:0001369

Meningitis

Very frequent (80-99%)HP:0001287

Migraine headache

Very frequent (80-99%)HP:0002076

Muscle pain

Very frequent (80-99%)HP:0003326

Nausea and vomiting

Very frequent (80-99%)HP:0002017

Papillitis

Very frequent (80-99%)HP:0001085

Papules

Very frequent (80-99%)HP:0200034

Pseudopapilledema

Very frequent (80-99%)HP:0000538

Pseudotumor cerebri

Very frequent (80-99%)HP:0002516

Pyrexia

Very frequent (80-99%)HP:0001945

Sensorineural deafness

Very frequent (80-99%)HP:0000407

Tiredness

Very frequent (80-99%)HP:0012378

Uveitis

Very frequent (80-99%)HP:0000554

Abnormal skeletal development

Frequent (30-79%)HP:0002652

Anterior bulging of the globe of eye

Frequent (30-79%)HP:0000520

Edema

Frequent (30-79%)HP:0000969

Enlarged liver

Frequent (30-79%)HP:0002240

Eosinophilia

Frequent (30-79%)HP:0001880

Related Conditions

Arthritis(parent)

Cryopyrin associated periodic syndrome(parent)

Quick Facts

SNOMED CT: 239826001
UMLS CUI: C0409818
Fully Specified Name: Chronic infantile neurological, cutaneous and articular syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 30

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.