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Disease Hypobetalipoproteinemia, Familial, Apolipoprotein B

Name Hypobetalipoproteinemia, Familial, Apolipoprotein B
Synonyms Abetalipoproteinemia, Normotriglyceridemic, Steinbert Type | Apolipoprotein B Deficiencies | Apolipoprotein B Deficiency | Apolipoprotein B Deficiency Disease | Hypobetalipoproteinemia, Familial, Apo B
Definition 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.
Categories Metabolic disease
MeSH® ID D052476

Top ↑ Ancestors

DiseasesNutritional and Metabolic Diseases Has associated chemicals Has associated genes Has associated exposure references Metabolic Diseases Has associated chemicals Has associated genes Has associated exposure references Lipid Metabolism Disorders Has associated chemicals Has associated genes Has associated exposure references Dyslipidemias Has associated chemicals Has associated genes Has associated exposure references Hypolipoproteinemias Has associated chemicals Has associated genes Hypobetalipoproteinemias Has associated chemicals Has associated genes Hypobetalipoproteinemia, Familial, Apolipoprotein B Has associated chemicals Has associated genes

Top ↑ Descendants

Hypobetalipoproteinemia, Familial, Apolipoprotein B Has associated chemicals Has associated genes
  Hypobetalipoproteinemia, Familial