OnlineIMD

21.9.1    Disorders of cobalamin absorption and transport

  • Type
    Group
  • Disease group(s)
    • 21.9    Disorders of cobalamin metabolism
  • Child entries
    • Hereditary intrinsic factor deficiency
    • Imerslund-Gräsbeck disease
    • Haptocorrin deficiency
    • Transcobalamin II deficiency
    • Transcobalamin receptor deficiency