← Back to Conditions

Late-onset junctional epidermolysis bullosa

disorder
SNOMED 719432000CUI C4304724

Overview

Late-onset junctional 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.

Adermatoglyphia
Frequent (30-79%)HP:0007455
Anonychia
Frequent (30-79%)HP:0001798
Dysplasia of tooth enamel
Frequent (30-79%)HP:0006297
Dystrophic nails
Frequent (30-79%)HP:0008404
Fragile skin
Frequent (30-79%)HP:0001030
Skin bullae
Frequent (30-79%)HP:0008066
Bullae of oral mucosa
Occasional (5-29%)HP:0200097
Dental cavities
Occasional (5-29%)HP:0000670
Hypoplastic dermoepidermal hemidesmosomes
Occasional (5-29%)HP:0020117
Localised skin lesion
Occasional (5-29%)HP:0011355
Profuse sweating
Occasional (5-29%)HP:0000975

Quick Facts

SNOMED CT
719432000
UMLS CUI
C4304724
Fully Specified Name
Late-onset junctional epidermolysis bullosa (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
11
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.