Autosomal dominant lamellar ichthyosis

disorder

SNOMED 254164007CUI C0432304

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.

Congenital lamellar ichthyosis

HP:0007479

Epidermal hyperkeratosis

HP:0000962

Skin itching

HP:0000989

Related Conditions

Lamellar ichthyosis(parent)

Congenital non bullous ichthyosiform erythroderma(parent)

Autosomal dominant ichthyosis(parent)

Quick Facts

SNOMED CT: 254164007
UMLS CUI: C0432304
Fully Specified Name: Autosomal dominant lamellar ichthyosis (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 3

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.