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Autosomal recessive epidermolysis bullosa simplex

disorder
SNOMED 1156849001CUI C1832926

Overview

Autosomal recessive epidermolysis bullosa simplex is a disorder.

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

Related Conditions

Epidermolysis bullosa simplex due to BP230 deficiency(child)
Epidermolysis bullosa simplex due to exophilin 5 deficiency(child)
Epidermolysis bullosa simplex with muscular dystrophy(child)
KRT14 related epidermolysis bullosa simplex(child)
Epidermolysis bullosa simplex due to plakophilin deficiency(child)
Epidermolysis bullosa simplex with pyloric atresia(child)
Lethal acantholytic erosive disorder(child)
Lethal autosomal recessive epidermolysis bullosa simplex(child)
Epidermolysis bullosa simplex(parent)
Recessive hereditary disorder (autosomal)(parent)

Quick Facts

SNOMED CT
1156849001
UMLS CUI
C1832926
Fully Specified Name
Autosomal recessive 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.