Familial benign pemphigus

disorder

SNOMED 79468000CUI C0085106

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.

Epidermal hyperkeratosis

Very frequent (80-99%)HP:0000962

Erythema

Very frequent (80-99%)HP:0010783

Nikolsky's sign

Very frequent (80-99%)HP:0100792

Skin erosion

Very frequent (80-99%)HP:0200041

Skin vesicle

Very frequent (80-99%)HP:0200037

Related Conditions

Inherited disorder of keratinization(parent)

Chronic skin disease(parent)

Autosomal dominant hereditary disorder(parent)

Blister of skin(parent)

Acantholytic dermatosis(parent)

Quick Facts

SNOMED CT: 79468000
UMLS CUI: C0085106
Fully Specified Name: Familial benign pemphigus (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 5

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.