Treatments & Interventions
Related Conditions
Familial hypercholesterolemia - homozygous(child)
Familial hypercholesterolaemia - heterozygous(child)
Fredrickson type IIa hyperlipoproteinaemia(child)
Familial hypercholesterolaemia due to heterozygous LDL receptor mutation(child)
Familial hypercholesterolaemia due to genetic defect of apolipoprotein B(child)
Familial hypercholesterolaemia co-occurrent and due to combined heterozygous low density lipoprotein receptor and low density lipoprotein receptor adaptor protein 1 mutations(child)
Primary hypercholesterolemia(parent)
Quick Facts
- SNOMED CT
- 398036000
- UMLS CUI
- C0020445
- Fully Specified Name
- Familial hypercholesterolemia (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- Known Treatments
- 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.