Autosomal dominant epidermolysis bullosa simplex

disorder

SNOMED 398170002CUI C0268375

Overview

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

Related Conditions

Epidermolysis bullosa simplex, Ogna type(child)

Epidermolysis bullosa simplex with circinate migratory erythema(child)

Weber-Cockayne syndrome(child)

Intermediate epidermolysis bullosa simplex with cardiomyopathy(child)

Epidermolysis bullosa simplex(parent)

Autosomal dominant hereditary disorder(parent)

Quick Facts

SNOMED CT: 398170002
UMLS CUI: C0268375
Fully Specified Name: Autosomal dominant epidermolysis bullosa simplex (disorder)
Specialists: 0
Diagnostic Biomarkers: 0

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.