familial apolipoprotein A5 deficiency

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.

Also known as: familial APOA5 deficiency; familial apolipoprotein A-V deficiency