An autosomal dominant genetic condition caused by mutation(s) in the CETP gene, encoding cholesteryl ester transfer protein. Affected individuals may have increased longevity due to decreased risk of coronary heart disease.
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familial hyperlipidemia
MONDO:0001336
familial hypercholesterolemia
MONDO:0005439
cholesterol-ester transfer protein deficiency
MONDO:0007744
familial lipoprotein lipase deficiency
MONDO:0009387
hypercholesterolemia, familial, 4
MONDO:0011374
hyperlipidemia due to hepatic triglyceride lipase deficiency
MONDO:0013533