(Q2349695)

English

familial lipoprotein lipase deficiency

familial hyperlipemia characterized by a deficiency of the enzyme lipoprotein lipase and the subsequent build up of chylomicrons and increased plasma concentration of triglycerides

  • Fredrickson type I hyperlipoproteinemia (disorder)
  • Fredrickson type I lipaemia
  • familial LPL deficiency
  • familial hyperchylomicronemia (disorder)
  • familial hyperlipoproteinemia type I
  • familial lipoprotein lipase deficiency (disorder) [Ambiguous]
  • familial lipoprotein lipase deficiency with type I phenotype
  • hypercholesterinaemic xanthomatosis
  • hyperchylomicronemia
  • mixed hyperglyceridemia
  • Fredrickson type I hyperlipoproteinemia
  • familial chylomiconemia syndrome
  • Hyperlipemia, Essential Familial
  • HYPERLIPOPROTEINEMIA, TYPE I
  • Familial fat-induced hypertriglyceridemia
  • Lipoprotein Lipase Deficiency
  • Lpl Deficiency
  • Hyperlipoproteinemia, Type 1A
  • Lipd Deficiency
  • Familial hyperchylomicronemia
  • Endogenous hypertriglyceridaemia
  • Type I hyperlipoproteinemia
  • Lipoprotein lipase deficiency, familial
  • Hyperlipemia, Idiopathic, Burger-Grutz Type
  • Chylomicronemia, Familial
  • Burger-Grutz syndrome
  • Lipase D Deficiency
  • Hyperchylomicronemia, Familial
  • familial chylomicronemia syndrome
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