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Hyperalphalipoproteinemia

MONDO:0015903

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.

Also known as: HALP1

11 clinical trials for this condition and its sub-types.

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Sub-types

Cholesterol-ester transfer protein deficiency (0) Hyperlipidemia due to hepatic triglyceride lipase deficiency (0)

Broader categories

Disease (618) Hyperlipidemia (264) Metabolic disease (215) Human disease (14) Hyperlipoproteinemia (7) Disease by developmental or physiological process (0)
Trials to join now! 8 Not yet recruiting 1 Not yet finished but already full! 1 Completed 1
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