Riboflavin transporter 2 deficiency

Synonym(s)
- Brown-Vialetto-van Laere syndrome type 2
Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- SLC52A2 / Solute Carrier Family 52 Member 2
  8q24.3
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Riboflavin transporter 2
Disease group(s)
- 21.3 Disorders of riboflavin metabolism