Overview
Acral dystrophic 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.
Abnormality of the lower limb
Frequent (30-79%)HP:0002814
Acral blistering
Frequent (30-79%)HP:0031045
Crusting erythematous dermatitis
Frequent (30-79%)HP:0007473
Cutaneous photosensitivity
Frequent (30-79%)HP:0000992
Dystrophic fingernails
Frequent (30-79%)HP:0008391
Dystrophic toenails
Frequent (30-79%)HP:0001810
Erythema
Frequent (30-79%)HP:0010783
Erythematous plaque
Frequent (30-79%)HP:0025474
Esophageal stricture
Frequent (30-79%)HP:0002043
Fragile skin
Frequent (30-79%)HP:0001030
Milia
Frequent (30-79%)HP:0001056
Palmoplantar keratosis
Frequent (30-79%)HP:0000972
Poikiloderma
Frequent (30-79%)HP:0001029
Skin bullae
Frequent (30-79%)HP:0008066
Skin degeneration
Frequent (30-79%)HP:0004334
Telangiectasia
Frequent (30-79%)HP:0001009
Thin skin
Frequent (30-79%)HP:0000963
Abnormality of the elbow
Occasional (5-29%)HP:0009811
Abnormality of the knee
Occasional (5-29%)HP:0002815
Recurrent loss of toenails and fingernails
Occasional (5-29%)HP:0008390
Quick Facts
- SNOMED CT
- 733638006
- UMLS CUI
- C4518087
- Fully Specified Name
- Acral dystrophic epidermolysis bullosa (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 20
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.