SLC2A2, solute carrier family 2 member 2, 6514

N. diseases: 123; N. variants: 32
Disease: Fanconi Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0015624
Disease: Fanconi Syndrome
Fanconi Syndrome 		0.300 Biomarker disease CTD_human The mutation spectrum of the facilitative glucose transporter gene SLC2A2 (GLUT2) in patients with Fanconi-Bickel syndrome. 11810292 2002