OnlineIMD

Sulfate transporter deficiency

  • Type
    Disease
  • External link(s)
    • IEMbase
  • Gene
    • SLC26A2 / Solute Carrier Family 26 Member 2
      • 5q32
      • OMIM
      • GnomAD
      • Ensembl
      • HGNC
      • VMH
      • LOVD
  • Gene product
    • Sulfate anion transporter
  • Disease group(s)
    • 18.2.3    Disorders of glycosaminoglycan synthesis and O-xylosylation
  • Child entries
    • Multiple epiphyseal dysplasia type 4
    • Atelosteogenesis type 2
    • Achondrogenesis type 1B
    • Diastrophic dysplasia