SLC2A6, solute carrier family 2 member 6, 11182

N. diseases: 39; N. variants: 2
Disease: Dementia, familial Danish ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1861735
Disease: Dementia, familial Danish
Dementia, familial Danish 		0.010 Biomarker disease BEFREE Notably, ITM2B variants linked to familial Danish dementia and retinal dystrophy significantly attenuated the inhibition of GLUT9-mediated urate influx. 31695625 2019