LPL, lipoprotein lipase, 4023

N. diseases: 290; N. variants: 116
Disease: Congenital chromosomal disease ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease 		0.030 Biomarker group BEFREE In multivariate analysis, cytogenetic aberrations and LPL had significant impact on survival. 27757836 2017
CUI: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease 		0.030 AlteredExpression group BEFREE Higher LPL level was found in patients with unfavorable cytogenetic aberrations (deletion in 17p13 or 11q22) in contrast to lower level in good risk cytogenetics (deletion in 13q as the sole abnormality) (r = 0.404, P = 0.002). 18616755 2009
CUI: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease 		0.030 GeneticVariation group BEFREE Loss of a part of chromosome 8p22, containing the gene LPL and amplifications of the field 8q24 comprising the c-myc oncogene are the most frequent chromosomal aberrations in prostate cancer. 17319789 2007