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Medical Subject Headings

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Sisällön kieli

Käsitteen tiedot

... > Nutritional and Metabolic Diseases > Metabolic Diseases > Lipid Metabolism Disorders > Lipid Metabolism, Inborn Errors > Hypolipoproteinemias > Hypobetalipoproteinemias > Hypobetalipoproteinemia, Familial, Apolipoprotein B
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Lipid Metabolism, Inborn Errors > Hypolipoproteinemias > Hypobetalipoproteinemias > Hypobetalipoproteinemia, Familial, Apolipoprotein B
... > Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Lipid Metabolism, Inborn Errors > Hypolipoproteinemias > Hypobetalipoproteinemias > Hypobetalipoproteinemia, Familial, Apolipoprotein B
... > Nutritional and Metabolic Diseases > Metabolic Diseases > Lipid Metabolism Disorders > Dyslipidemias > Hypolipoproteinemias > Hypobetalipoproteinemias > Hypobetalipoproteinemia, Familial, Apolipoprotein B

Käytettävä termi

Hypobetalipoproteinemia, Familial, Apolipoprotein B  

Tyyppi

  • Topical Descriptor

Yläkäsite

Ohjaustermit

  • Abetalipoproteinemia, Normotriglyceridemic, Steinbert Type
  • Apolipoprotein B Deficiencies
  • Apolipoprotein B Deficiency
  • Apolipoprotein B Deficiency Disease
  • Hypobetalipoproteinemia, Familial, Apo B

Käyttöhuomautus

  • An autosomal dominant disorder of lipid metabolism. It is caused by mutations of APOLIPOPROTEINS B, main components of CHYLOMICRONS and BETA-LIPOPROTEINS (low density lipoproteins or LDL). Features include abnormally low LDL, normal triglyceride level, and dietary fat malabsorption.

Huomautus muutoshistoriasta

  • 2007; for APOLIPOPROTEIN B DEFICIENCY DISEASE use ABETALIPOPROTEINEMIA 2000-2006

Muunkieliset termit

URI

http://www.yso.fi/onto/mesh/D052476

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RDF/XML TURTLE JSON-LD Luotu 5.7.2006, viimeksi muokattu 11.4.2022