Klinische FragestellungLipoprotein-Lipase Defizienz, Differentialdiagnose

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illness_ClinicalComment_ LP7688

• Alias: Burger-Grutz syndrome
• Alias: Chylomikronämie-Syndrom, familiäres
• Alias: Endogenous hypertriglyceridaemia
• Alias: Familial LPL deficiency
• Alias: Familial Lipoprotein Lipase Deficiency
• Alias: Familial chylomicromenia [syndrome]
• Alias: Familial fat-induced hypertriglyceridemia
• Alias: Familial hyperchylomicronemia
• Alias: Hyperlipoproteinemia type I
• Alias: Hyperlipoproteinemia type Ia
• Alias: LIPD deficiency
• Alias: Lipase D deficiency
• Alias: Lipoprotein lipase deficiency, familial
• Allelic: Alzheimer disease 2 (APOE)
• Allelic: Alzheimer disease, protection against, due to APOE3-Christchurch (APOE)
• Allelic: Coronary artery disease, severe, susceptibility to (APOE)
• Allelic: High density lipoprotein cholesterol level QTL 11 (LPL)
• Allelic: Lipoprotein glomerulopathy (APOE)
• Allelic: Macular degeneration, age-related (APOE)
• Allelic: Sea-blue histiocyte disease (APOE)
• Combined hyperlipidemia, familial (LPL)
• Hypercholesterolemia, familial, 2 (APOB)
• Hyperchylomicronemia, late-onset (APOA5)
• Hyperlipoproteinemia, type ID (GPIHBP1)
• Hyperlipoproteinemia, type III (APOE)
• Hyperlipoproteinemia, type Ib (APOC2)
• Hypertriglyceridemia 2 (CREB3L3)
• Hypertriglyceridemia, susceptibility to (APOA5)
• Hypertriglyceridemia, transient infantile (GPD1)
• Hypobetalipoproteinemia (APOB)
• Lipase deficiency, combined (LMF1)
• Lipoprotein lipase deficiency (LPL)