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- Apolipoprotein e variants
- Autosomal dominant hypercholesterolemia with pcsk9 mutation
- Familial defective apolipoprotein b 100
- Familial dysbetalipoproteinemia
- Familial hypobetaliproteinemia
- Fredrickson classification
- Hereditary polygenic hypercholesterolemia
- Hypercholesterolemia familial autosomal dominant
- Hyperlipoproteinemia secondary
- Hypertriglyceridemia familial
- Lecithin-cholesterol acyltransferase deficiency
- Lipoprotein (a) hyperlipoproteinemia
- Serine protease
- Xanthoma tuberosum