familial lipoprotein lipase deficiency (Q2349695)

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Human disease
  • familial lipoprotein lipase deficiency
  • 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
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Language Label Description Also known as
English
familial lipoprotein lipase deficiency
Human disease
  • familial lipoprotein lipase deficiency
  • 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

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