Epidermolysis bullosa simplex with circinate migratory erythema

disorder

SNOMED 716700003CUI C1836284

Overview

Epidermolysis bullosa simplex with circinate migratory erythema 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.

Intra-epidermal blistering

Always present (100%)HP:0033802

Acral blistering

Frequent (30-79%)HP:0031045

Blister

Frequent (30-79%)HP:0008066

Erythema chronicum migrans

Frequent (30-79%)HP:0031180

Fair skin

Frequent (30-79%)HP:0007513

Junctional split

Frequent (30-79%)HP:0003341

Parakeratosis

Frequent (30-79%)HP:0001036

Patchy darkened skin

Frequent (30-79%)HP:0000953

Patchy hyperpigmentation

Frequent (30-79%)HP:0005585

Skin fragility with non-scarring blistering

Frequent (30-79%)HP:0007585

Skin itching

Frequent (30-79%)HP:0000989

Skin vesicle

Frequent (30-79%)HP:0200037

Abnormality of the knee

Occasional (5-29%)HP:0002815

Abnormality of the neck

Occasional (5-29%)HP:0000464

Generalized reticulate brown pigmentation

Occasional (5-29%)HP:0007599

Pretibial blistering

Occasional (5-29%)HP:0012221

Related Conditions

Autosomal dominant epidermolysis bullosa simplex(parent)

Quick Facts

SNOMED CT: 716700003
UMLS CUI: C1836284
Fully Specified Name: Epidermolysis bullosa simplex with circinate migratory erythema (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 16

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.