Preferred Name |
Hyperlipoproteinemia Type I |
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Synonyms |
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ID |
http://www.semanticweb.org/ontologies/STO.owl#b52086a3_8929_4f3b_a866_6df368dadbc6 |
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hasDbXref | ||
isDefinedBy |
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. |
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label |
Hyperlipoproteinemia Type I |
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prefixIRI |
b52086a3_8929_4f3b_a866_6df368dadbc6 |
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prefLabel |
Hyperlipoproteinemia Type I |
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synonyms |
Lipoprotein Lipase Deficiency Familial Chylomicronemia Apolipoprotein C II Deficiency Familial LPL Deficiency Burger Grutz Syndrome Lipoprotein Lipase Deficiencies Familial Hyperlipoproteinemia Type 1 Type I Hyperlipoproteinemia Familial Fat Induced Hypertriglyceridemia Familial Hyperchylomicronemia Familial LPL Deficiencies Lipase D Deficiencies LIPD Deficiency C-II Anapolipoproteinemias Burger-Grutz Syndromes Type I Hyperlipoproteinemias Familial Hyperchylomicronemias C-II Anapolipoproteinemia Familial Lipoprotein Lipase Deficiency Lipase D Deficiency |
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subClassOf |
http://www.semanticweb.org/ontologies/STO.owl#a024a295_0176_4255_8207_24a18336930b |