Hypobetalipoproteinemia, Familial, Apolipoprotein B

Source:http://linkedlifedata.com/resource/umls/id/C1704299

MSH: 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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