LBP, lipopolysaccharide binding protein, 3929

N. diseases: 156; N. variants: 7
Disease: Congenital glucose-galactose malabsorption ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0268186
Disease: Congenital glucose-galactose malabsorption
Congenital glucose-galactose malabsorption 		0.010 AlteredExpression disease BEFREE In addition, GGM significantly increased the levels of butyric acid and caproic acid, and reduced the levels of LBP in serum. 30256506 2019