OnlineIMD

Hereditary intrinsic factor deficiency

  • Type
    Disease
  • External link(s)
    • Orphanet
    • IEMbase
  • Gene
    • CBLIF / CBL proto-oncogene like F
      • 11q12.1
      • OMIM
      • GnomAD
      • Ensembl
      • HGNC
      • VMH
      • LOVD
  • Gene product
    • E3 ubiquitin-protein ligase CBL-like protein
  • Disease group(s)
    • 21.9.1    Disorders of cobalamin absorption and transport