- Type 1 hereditary hemochromatosis
- Type 2 hereditary hemochromatosis (juvenile hemochromatosis)
- Type 3 hereditary hemochromatosis (transferrin receptor 2 [TFR2] mutation hemochromatosis)
- Type 4 hereditary hemochromatosis (ferroportin disease)
- Transferrin deficiency (hypotransferrinemia or atransferrinemia) and ceruloplasmin deficiency (aceruloplasminemia)
- Etiology references
- Pathophysiology
- Symptoms and Signs
- Key Points