Digenic haemochromatosis

disorder

SNOMED 1299153008CUI C5816744

Overview

Digenic haemochromatosis is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Related Conditions

Metabolic and genetic disorder affecting the liver(parent)

Hereditary hemochromatosis(parent)

Digestive system hereditary disorder(parent)

Inborn error of metabolism(parent)

Disorder of digestive system specific to fetus OR newborn(parent)

Quick Facts

SNOMED CT: 1299153008
UMLS CUI: C5816744
Fully Specified Name: Digenic hemochromatosis (disorder)
Specialists: 0
Diagnostic Biomarkers: 0

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.