cholesterol-ester transfer protein deficiency

Summary
Synonym
  • CEPT deficiency
  • familial hyperalphalipoproteinemia
Definition
A lipid metabolism disorder characterized by elevated levels of alpha-lipoprotein in the blood.
Super Class
lipid metabolism disorder
External Links
Disease Ontology
DOID:0111368
ORDO
WikiPathways (from TogoID)
Related Genes
Displaying all 5 entries
Gene ID Gene Symbol Description Source
2590 GALNT2 polypeptide N-acetylgalactosaminyltransferase 2
3931 LCAT lecithin-cholesterol acyltransferase
3990 LIPC lipase C, hepatic type
4023 LPL lipoprotein lipase
9388 LIPG lipase G, endothelial type

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024