Congenital lethal erythroderma

disorder

SNOMED 722391005CUI C1856898

Overview

Congenital lethal erythroderma 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.

Congenital exfoliative erythroderma

Very frequent (80-99%)HP:0007381

Hives

Very frequent (80-99%)HP:0001025

Ichthyosiform abnormality of the skin

Very frequent (80-99%)HP:0008064

Intestinal malabsorption

Very frequent (80-99%)HP:0002024

Low albumin

Very frequent (80-99%)HP:0003073

Poor weight gain

Very frequent (80-99%)HP:0001508

Respiratory insufficiency

Very frequent (80-99%)HP:0002093

Xerosis

Very frequent (80-99%)HP:0000958

Related Conditions

Congenital disease(parent)

Recessive hereditary disorder (autosomal)(parent)

Hereditary disorder of the integument(parent)

Erythroderma(parent)

Inflammatory dermatosis(parent)

Fetal and/or neonatal disorder of integument(parent)

Quick Facts

SNOMED CT: 722391005
UMLS CUI: C1856898
Fully Specified Name: Congenital lethal erythroderma (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 8

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.