hyperalphalipoproteinemia
MONDO:0015903Mondo
Findings
No curated finding names hyperalphalipoproteinemia yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
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.
Definition from the Mondo Disease Ontology (MONDO:0015903), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
Other names
1 name
Resolves to: hyperalphalipoproteinemia
- Also called
- HALP1