Browse

Explore conditions, clinical trials, and the organisations running them.

← All categories

Up to: Hyperlipidemia · Hyperlipoproteinemia

Hyperalphalipoproteinemia

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.

0 trials tagged with this condition →