Overview
Acquired epidermolysis bullosa 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.
Abnormal hair morphology
Very frequent (80-99%)HP:0001595
Blister
Very frequent (80-99%)HP:0008066
Milia
Frequent (30-79%)HP:0001056
Atypical scarring
Occasional (5-29%)HP:0000987
Diabetes mellitus
Occasional (5-29%)HP:0000819
Dystrophic nails
Occasional (5-29%)HP:0008404
Inflammation of the large intestine
Occasional (5-29%)HP:0002037
Melanoderma
Occasional (5-29%)HP:0000953
Skin itching
Occasional (5-29%)HP:0000989
Upset stomach
Occasional (5-29%)HP:0002027
Related Conditions
Epidermolysis bullosa acquisita, classical acral type(child)
Epidermolysis bullosa acquisita, bullous pemphigoid-like(child)
Epidermolysis bullosa acquisita, cicatricial pemphigoid-like(child)
Epidermolysis bullosa acquisita, Brunsting-Perry type(child)
Epidermolysis bullosa acquisita, oral mucosal involvement(child)
Drug-induced epidermolysis bullosa acquisita(child)
Autoimmune skin disease(parent)
Chronic skin disease(parent)
Chronic disease of immune function(parent)
Degenerative skin disorder(parent)
Blister of skin(parent)
Quick Facts
- SNOMED CT
- 2772003
- UMLS CUI
- C0079293
- Fully Specified Name
- Acquired epidermolysis bullosa (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.