5.02.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
NOMS
Disorders of neuromodulators and other small molecules
