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GTR Home > Conditions/Phenotypes > Familial type 5 hyperlipoproteinemia

Familial type 5 hyperlipoproteinemia

Synonyms
Hyperchylomicronemia late onset; Hyperchylomicronemia with hyperprebetalipoproteinemia, familial; Hyperlipemia combined fat and carbohydrate-induced; Hyperlipemia mixed; Hyperlipidemia type V; Hyperlipoproteinemia Type V; Hyperlipoproteinemia type 5
Modes of inheritance
Autosomal recessive inheritance (Orphanet)

Summary

A severe type of hyperlipidemia, sometimes familial, that is characterized by the elevation of both plasma chylomicrons and triglycerides contained in very-low-density lipoproteins. Type V hyperlipoproteinemia is often associated with diabetes mellitus and is not caused by reduced lipoprotein lipase activity as in hyperlipoproteinemia type I. [from MONDO]

Available tests

18 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (18 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: APOAV, RAP3, APOA5
    Summary: apolipoprotein A5

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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