familial apolipoprotein A5 deficiency

Summary
Synonym
  • familial APOA5 deficiency
  • familial apolipoprotein A-V deficiency
Definition
A familial chylomicronemia syndrome characterized by hyperchylomicronemia, elevated levels of very low density lipoprotein, and decreased LDL and HDL levels after fasting that has_material_basis_in heterozygous mutation in the APOA5 gene on chromosome 11q23.3.
Super Class
autosomal dominant disease familial chylomicronemia syndrome
External Links
Disease Ontology
DOID:0111421
Mondo Disease Ontology
ORDO
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
4023 LPL lipoprotein lipase
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
P06858 Lipoprotein lipase

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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