LIPC, lipase C, hepatic type, 3990

N. diseases: 120; N. variants: 95
Disease: Lipid Metabolism, Inborn Errors ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0023772
Disease: Lipid Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors 		0.300 Biomarker group CTD_human The -514 C->T hepatic lipase promoter region polymorphism and plasma lipids: a meta-analysis. 15292318 2004
CUI: C0023772
Disease: Lipid Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors 		0.300 Biomarker group CTD_human A hepatic lipase gene mutation associated with heritable lipolytic deficiency. 1671786 1991
CUI: C0023772
Disease: Lipid Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors 		0.300 Biomarker group CTD_human Compound heterozygosity for mutant hepatic lipase in familial hepatic lipase deficiency. 1883393 1991