OnlineIMD

Congenital sucrase-isomaltase deficiency

  • Type
    Disease
  • External link(s)
    • Orphanet
    • IEMbase
    • VMH
  • Gene
    • SI / Sucrase-Isomaltase
      • 3q26.1
      • OMIM
      • GnomAD
      • Ensembl
      • HGNC
      • VMH
      • LOVD
  • Gene product
    • Sucrase-isomaltase
  • Disease group(s)
    • 3.6        Disorders of carbohydrate transmembrane transport and absorption