Urate transporter 1 deficiency

Synonym(s)
- Hereditary renal hypouricemia type 1
Type

Disease
External link(s)
- IEMbase
Gene
- SLC22A12 / Solute Carrier Family 22 Member 12
  11q13.1
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Urate transporter 1
Parent entry
- Hereditary renal hypouricemia