Hypobetalipoproteinemia, Familial, Apolipoprotein B

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

Statements in which the resource exists.
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umls-concept:C1704299skos:definitionMSH: 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.lld:umls
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