SLC2A2, solute carrier family 2 member 2, 6514

N. diseases: 123; N. variants: 32
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 GeneticVariation disease BEFREE Mutations in SGLT1 are associated with glucose-galactose malabsorption, SGLT2 with familial renal glucosuria (FRG), and GLUT2 with Fanconi-Bickel syndrome. 19965550 2010