Proton-coupled folate transporter deficiency

Synonym(s)
- Hereditary folate malabsorption
Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- SLC46A1 / Solute Carrier Family 46 Member 1
  17q11.2
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Folate transporter
Disease group(s)
- 21.8 Disorders of folate metabolism