Epidermodysplasia verruciformis

disorder

SNOMED 19138001CUI C0014522

Overview

Epidermodysplasia verruciformis 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.

Dysseborrheic dermatitis

Very frequent (80-99%)HP:0001051

Immunological abnormality

Very frequent (80-99%)HP:0002715

Papules

Very frequent (80-99%)HP:0200034

Pimple

Very frequent (80-99%)HP:0200039

Skin infections, recurrent

Very frequent (80-99%)HP:0001581

Skin plaque

Very frequent (80-99%)HP:0200035

Warts

Very frequent (80-99%)HP:0200043

Hypopigmented skin patches

Frequent (30-79%)HP:0001053

Multiple flat light-brown marks on skin

Frequent (30-79%)HP:0007565

Squamous cell carcinoma

Occasional (5-29%)HP:0002860

Teleangiectasia of the skin

Occasional (5-29%)HP:0100585

Basal cell nevus

HP:0002671

Laboratory abnormality

HP:0001939

Related Conditions

Recessive hereditary disorder (autosomal)(parent)

Skin lesion(parent)

Viral infection of skin(parent)

Hereditary disorder of the integument(parent)

Viral wart(parent)

Quick Facts

SNOMED CT: 19138001
UMLS CUI: C0014522
Fully Specified Name: Epidermodysplasia verruciformis (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 13

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.