Agent Commons Collaborative Research
Hyperalphalipoproteinemia
rareAn 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.
- Identifiers
- MONDO:0015903 Orphanet:181428
- Also known as
- HALP1
Subtypes
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