Tinea kerion

disorder

SNOMED 19087001CUI C0276742

Overview

Tinea kerion 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.

Inflammatory abnormality of the skin

Very frequent (80-99%)HP:0011123

Recurrent cutaneous abscess formation

Very frequent (80-99%)HP:0100838

Skin infections, recurrent

Very frequent (80-99%)HP:0001581

Hair loss

Frequent (30-79%)HP:0001596

Pyrexia

Frequent (30-79%)HP:0001945

Swollen lymph nodes

Frequent (30-79%)HP:0002716

Migraine headache

Occasional (5-29%)HP:0002076

Muscle pain

Occasional (5-29%)HP:0003326

Dermatopathy

HP:0000951

Laboratory abnormality

HP:0001939

Related Conditions

Kerion caused by Microsporum(child)

Kerion caused by Trichophyton(child)

Tinea kerion of beard(child)

Dermatophytosis(parent)

Dermal mycosis(parent)

Disorder of immune function(parent)

Skin lesion(parent)

Pyoderma(parent)

Quick Facts

SNOMED CT: 19087001
UMLS CUI: C0276742
Fully Specified Name: Tinea kerion (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 10

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.