Familial hypercholesterolaemia due to homozygous LDL receptor mutation

disorder

SNOMED 403830007CUI C1304504

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Related Conditions

Familial hypercholesterolemia - homozygous(parent)

Quick Facts

SNOMED CT: 403830007
UMLS CUI: C1304504
Fully Specified Name: Familial hypercholesterolemia due to homozygous low density lipoprotein receptor mutation (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.