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Epidermolysis bullosa pruriginosa

disorder
SNOMED 403810008CUI C1275114

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Skin bullae
Very frequent (80-99%)HP:0008066
Skin itching
Very frequent (80-99%)HP:0000989
Abnormality of the elbow
Frequent (30-79%)HP:0009811
Abnormality of the wrist
Frequent (30-79%)HP:0003019
Dystrophic nails
Frequent (30-79%)HP:0008404
Lichenification
Frequent (30-79%)HP:0100725
Pretibial blistering
Frequent (30-79%)HP:0012221
Skin plaque
Frequent (30-79%)HP:0200035
Abnormal forearm morphology
Occasional (5-29%)HP:0002973
Abnormal toenail morphology
Occasional (5-29%)HP:0008388
Abnormality of head or neck
Occasional (5-29%)HP:0000152
Epidermal hyperkeratosis
Occasional (5-29%)HP:0000962
Junctional split
Occasional (5-29%)HP:0003341
Milia
Occasional (5-29%)HP:0001056
Papules
Occasional (5-29%)HP:0200034
Scarring
Occasional (5-29%)HP:0100699
Skin degeneration
Occasional (5-29%)HP:0004334
Subcutaneous nodule
Occasional (5-29%)HP:0001482
Thin, atrophic scars
Occasional (5-29%)HP:0001075
High immunoglobulin E
Very rare (1-4%)HP:0003212
Fragile skin
HP:0001030
Nail dysplasia
HP:0002164

Quick Facts

SNOMED CT
403810008
UMLS CUI
C1275114
Fully Specified Name
Epidermolysis bullosa pruriginosa (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
22
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.