OnlineIMD

Hartnup disease

  • Type
    Disease
  • External link(s)
    • Orphanet
    • IEMbase
    • VMH
  • Gene
    • SLC6A19 / Solute Carrier Family 6 Member 19
      • 5p15.33
      • OMIM
      • GnomAD
      • Ensembl
      • HGNC
      • VMH
      • LOVD
  • Gene product
    • Neutral amino acid transporter B(0)
  • Disease group(s)
    • 1.11    Disorders of amino acid transport