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hypobetalipoproteinémia s deficitom apolipoproteínu B, familiárna

Subject h.	hypobetalipoproteinémia s deficitom apolipoproteínu B, familiárna
Subject h.	Hypobetalipoproteinemia, Familial, Apolipoprotein B
Entry terms	deficit apolipoproteínu B
English X references	Apolipoprotein B Deficiency
Scope note in English	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.
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