HAO2, hydroxyacid oxidase 2, 51179

N. diseases: 22; N. variants: 0
Disease: Congenital Hyperinsulinism ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3888018
Disease: Congenital Hyperinsulinism
Congenital Hyperinsulinism 		0.010 Biomarker disease BEFREE Glycolate oxidase deficiency in a patient with congenital hyperinsulinism and unexplained hyperoxaluria. 28752386 2017