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.

Epidermolysis bullosa simplex with circinate migratory erythema — Symptoms, Testing & Specialists | Ltrl | Ltrl