AGT, angiotensinogen, 183

N. diseases: 765; N. variants: 43
Disease: Urolithiasis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0451641
Disease: Urolithiasis
Urolithiasis 		0.010 AlteredExpression disease BEFREE Primary hyperoxaluria type I (PH1) is an inborn error of metabolism caused by deficiency of the hepatic enzyme alanine-glyoxylate aminotransferase (AGXT or AGT) which leads to overproduction of oxalate by the liver and subsequent urolithiasis and renal failure. 21119625 2011