SLC46A1, solute carrier family 46 member 1, 113235

N. diseases: 97; N. variants: 20
Disease: Folate Malabsorption, Hereditary ×
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C0342705
Disease: Folate Malabsorption, Hereditary
Folate Malabsorption, Hereditary 		disease Digestive System Diseases; Nutritional and Metabolic Diseases Disease or Syndrome 4 14 0.800 None 1.000 27 14 2001 2020