Riboflavin transporter 1 deficiency

Synonym(s)
- Transient riboflavin deficiency
Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- SLC52A1 / Solute Carrier Family 52 Member 1
  17p13.2
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Riboflavin transporter 1
Disease group(s)
- 21.3 Disorders of riboflavin metabolism