Non-Wilsonian hepatic copper toxicosis of infancy and childhood

disorder

SNOMED 715864007CUI C4274853

Overview

Non-Wilsonian hepatic copper toxicosis of infancy and childhood 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.

Cirrhosis

Always present (100%)HP:0001394

Copper accumulation in liver

Always present (100%)HP:0025321

Fatty liver

Frequent (30-79%)HP:0001397

Increased circulating copper concentration

Frequent (30-79%)HP:0032254

Increased urinary copper concentration

Frequent (30-79%)HP:0010839

Related Conditions

Cryptogenic cirrhosis(parent)

Disorder of liver due to disorder of mineral metabolism(parent)

Quick Facts

SNOMED CT: 715864007
UMLS CUI: C4274853
Fully Specified Name: Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 5

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.