Hyperlipoproteinemia Type I

Source:http://linkedlifedata.com/resource/umls/id/C0023817

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CSP: rare familial condition characterized by massive chylomicronemia and decreased levels of other lipoproteins; due to deficiency of lipoprotein lipase, an alkaline triglyceride hydrolase which catalyzes an important step in the extrahepatic removal of triglyceride-rich lipoproteins from the blood.,MSH: An inherited condition due to a deficiency of either LIPOPROTEIN LIPASE or APOLIPOPROTEIN C-II (a lipase-activating protein). The lack of lipase activities results in inability to remove CHYLOMICRONS and TRIGLYCERIDES from the blood which has a creamy top layer after standing.,NCI: A genetic disorder of lipoprotein metabolism caused by mutations in the LPL and apolipoprotein (apo) C-II genes. It is characterized by increased levels of chylomicrons and triglycerides in the blood.
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http://linkedlifedata.com/resource/umls/relation/R111754017, http://linkedlifedata.com/resource/umls/relation/R111754022, http://linkedlifedata.com/resource/umls/relation/R05669421, http://linkedlifedata.com/resource/umls/relation/R05669422, http://linkedlifedata.com/resource/umls/relation/R00890402, http://linkedlifedata.com/resource/umls/relation/R00890403, http://linkedlifedata.com/resource/umls/relation/R43984347, http://linkedlifedata.com/resource/umls/relation/R43984348, http://linkedlifedata.com/resource/umls/relation/R43984350, http://linkedlifedata.com/resource/umls/relation/R43984349, http://linkedlifedata.com/resource/umls/relation/R43984351, http://linkedlifedata.com/resource/umls/relation/R44004610, http://linkedlifedata.com/resource/umls/relation/R05691964, http://linkedlifedata.com/resource/umls/relation/R05691960, http://linkedlifedata.com/resource/umls/relation/R05691961, http://linkedlifedata.com/resource/umls/relation/R05691955, http://linkedlifedata.com/resource/umls/relation/R05691977, http://linkedlifedata.com/resource/umls/relation/R05691963, http://linkedlifedata.com/resource/umls/relation/R05691965
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