Urate voltage-driven efflux transporter 1 deficiency

Synonym(s)
- Hereditary renal hypouricemia type 2
Type

Disease
External link(s)
- IEMbase
Gene
- SLC2A9 / Solute Carrier Family 2 Member 9
  4p16.1
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Glucose transporter 9
Parent entry
- Hereditary renal hypouricemia