Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
The disposition to develop hight triglyceride levels is hereditary. Among others, the gene ANGPTL4 is responsible.
Hypertriglyceridemia
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APOA5
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APOE
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Combined lipase deficiency
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GPIHBP1
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LIPC
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LIPE
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LPL
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Plasma triglyceride level quantitative trait locus
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ANGPTL4
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Transient infantile hypertriglyceridemia
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| 1. |
Romeo S et al. (2009) Rare loss-of-function mutations in ANGPTL family members contribute to plasma triglyceride levels in humans. 
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| 2. |
Dewey FE et al. (2016) Inactivating Variants in ANGPTL4 and Risk of Coronary Artery Disease.
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| 3. |
et al. (2016) Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease.
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| 4. |
OMIM.ORG article Omim 615881
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