Subnetwork: Haemochromatosis and other iron disorders
Disease group/s: HFE-related hereditary hemochromatosis with established severe clinical expression or due to very rare mutations in HFE
Scope and Purpose: 5. Diagnosis and treatment
Patients' involvement?: No
Rigour of development: A - Evidence and consensus based
Some divergences with the European guidelines (namely on the value of the H63D variant).