hyperalphalipoproteinemia (Q56013772)
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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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | 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. |
Statements
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272.4
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C128806
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Identifiers
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