SLC20A2, solute carrier family 20 member 2, 6575

N. diseases: 104; N. variants: 36
Disease: Microcalcification ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0521174
Disease: Microcalcification
Microcalcification 		0.300 Biomarker phenotype CTD_human Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export. 25938945 2015