SLC46A1, solute carrier family 46 member 1, 113235

N. diseases: 97; N. variants: 20
Disease: Folate malabsorption ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2749650
Disease: Folate malabsorption
Folate malabsorption 		0.300 Biomarker phenotype GENOMICS_ENGLAND Neurological manifestations of folate transport defect: case report and review of the literature. 17641272 2007