- TypeGroup
- Disease group(s)
- Child entries
- Hemochromatosis
- HFE-hemochromatosis
- Hemojuvelin deficiency
- Hepcidin deficiency
- Transferrin receptor 2 deficiency
- Ferroportin deficiency
- BMP6 deficiency
- FTL-related disease
- Ferritin heavy chain dysregulation
- Hereditary ceruloplasmin deficiency
- Matriptrase 2 deficiency
- Hereditary transferrin deficiency
- Transferrin receptor deficiency
- Divalent metal transporter 1 deficiency
- Endosomal ferrireductase deficiency
- Hephaestin-like protein 1 deficiency