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Nutritional and Metabolic Diseases > Metabolic Diseases > Lipid Metabolism Disorders > Lipid Metabolism, Inborn Errors > Hyperlipoproteinemia Type I
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Lipid Metabolism, Inborn Errors > Hyperlipoproteinemia Type I
Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Lipid Metabolism, Inborn Errors > Hyperlipoproteinemia Type I
... > Nutritional and Metabolic Diseases > Metabolic Diseases > Lipid Metabolism Disorders > Dyslipidemias > Hyperlipidemias > Hyperlipoproteinemias > Hyperlipoproteinemia Type I

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Hyperlipoproteinemia Type I  

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Tipo

  • mesh:Descriptor

Definición

  • An inherited condition due to a deficiency of either LIPOPROTEIN LIPASE or APOLIPOPROTEIN C-II (a lipase-activating protein). The lack of lipase activities results in inability to remove CHYLOMICRONS and TRIGLYCERIDES from the blood which has a creamy top layer after standing.

Concepto genérico

Conceptos relacionados

Etiquetas alternativas

  • Burger-Grutz Syndrome
  • Chylomicronemia, Familial
  • Familial Hyperchylomicronemia
  • Familial Hyperlipoproteinemia Type 1
  • Familial Lipoprotein Lipase Deficiency
  • Familial LPL Deficiency
  • Hyperchylomicronemia, Familial
  • Hyperlipemia, Essential Familial
  • Hyperlipemia, Idiopathic, Burger-Grutz Type
  • Hyperlipoproteinemia, Type I
  • Hyperlipoproteinemia Type Ia
  • Hyperlipoproteinemia, Type Ia
  • Lipase D Deficiency
  • LIPD Deficiency
  • Lipoprotein Lipase Deficiency
  • Lipoprotein Lipase Deficiency, Familial

En otras lenguas

URI

http://data.loterre.fr/ark:/67375/JVR-XXZPJT41-C

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RDF/XML TURTLE JSON-LD Creado 23/4/79, última modificación 30/6/21