SLC26A6 deficiency

Synonym(s)
- Enteric hyperoxaluria and nephrolithiasis
Type

Disease
External link(s)
- IEMbase
Gene
- SLC26A6 / Solute Carrier Family 26 Member 6
  3p21.31
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Solute carrier family 26 member 6
Disease group(s)
- 13.3 Disorders of glyoxylate and oxalate metabolism