Overview
Junctional epidermolysis bullosa mitis 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 blistering of the skin
Very frequent (80-99%)HP:0008066
Abnormal skin colour
Very frequent (80-99%)HP:0001000
Bullae of oral mucosa
Very frequent (80-99%)HP:0200097
Congenital scars
Very frequent (80-99%)HP:0001057
Hair loss on scalp from scarring condition
Very frequent (80-99%)HP:0004552
Milia
Very frequent (80-99%)HP:0001056
Sparse body hair
Very frequent (80-99%)HP:0002231
Thin, atrophic scars
Very frequent (80-99%)HP:0001075
Anonychia
Frequent (30-79%)HP:0001798
Dystrophic nails
Frequent (30-79%)HP:0008404
Low number of red blood cells or haemoglobin
Frequent (30-79%)HP:0001903
Dysplasia of tooth enamel
Occasional (5-29%)HP:0006297
Growth failure
Occasional (5-29%)HP:0001510
Keratoderma
Occasional (5-29%)HP:0000982
Quick Facts
- SNOMED CT
- 254196004
- UMLS CUI
- C0432326
- Fully Specified Name
- Junctional epidermolysis bullosa mitis (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 14
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.