Hereditary skin peeling syndrome

disorder

SNOMED 724838009CUI C1849193

Overview

Hereditary skin peeling syndrome 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.

Eosinophilia

Always present (100%)HP:0001880

Erythroderma

Always present (100%)HP:0001019

High immunoglobulin E

Always present (100%)HP:0003212

Scaling skin

Always present (100%)HP:0040189

Skin itching

Always present (100%)HP:0000989

Fragile hair

Frequent (30-79%)HP:0002299

Hyperhidrosis of palms and soles

Frequent (30-79%)HP:0007410

Bronchial asthma

Occasional (5-29%)HP:0002099

Dystrophic nails

Occasional (5-29%)HP:0008404

Oncholysis

Occasional (5-29%)HP:0001806

Cleavage at junction of stratum corneum and stratum granulosum

HP:0034838

Decreased body height

Excluded (<1%)HP:0004322

Related Conditions

Generalized peeling skin syndrome(child)

Peeling skin syndrome, acral type(child)

Skin peeling disorder(parent)

Autosomal recessive ichthyosis(parent)

Quick Facts

SNOMED CT: 724838009
UMLS CUI: C1849193
Fully Specified Name: Hereditary skin peeling syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 12

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.