5.2.b

Disorders of iron metabolism

  • Hereditary hemochromatosis type 1
  • Hemojuvelin deficiency (Hereditary hemochromatosis type 2A)
  • Hepcidin deficiency (Hereditary hemochromatosis type 2B)
  • Transferrin receptor 2 deficiency (Hereditary hemochromatosis type 3)
  • Ferroportin deficiency (Hereditary hemochromatosis type 4; ferroportin disease)
  • BMP6 deficiency
  • Ferritin heavy chain dysregulation (Hereditary hemochromatosis type 5)
  • Ferritin light chain deficiency (Hereditary L-ferritin deficiency)
  • Ferritin light chain superactivity (Neuroferritinopathy; neurodegeneration with brain iron accumulation type 3)
  • Hyperferritinemia-cataract syndrome
  • Hereditary ceruloplasmin deficiency (Aceruloplasminemia)
  • Matriptrase 2 deficiency (Iron-refractory iron deficiency anemia – IRIDA)
  • Hereditary transferrin deficiency (Atransferrinemia)
  • Transferrin receptor deficiency (Immunodeficiency type 46)
  • Divalent metal transporter 1 deficiency (Hypochromic microcytic anemia with iron overload type 1)
  • Endosomal ferrireductase deficiency (Hypochromic microcytic anemia with iron overload type 2)
  • Hephaestin-like protein 1 deficiency

Subnetworks

Immagini SNW 344 x 258 px 1

NOMS

Disorders of neuromodulators and other small molecules

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