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EMQN best practice guidelines for the molecular genetic diagnosis of hereditary hemochromatosis (HH)

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: 2. Diagnosis

Patients' involvement?: No

Rigour of development: A - Evidence and consensus based

Link: https://www.ncbi.nlm.nih.gov/pubmed/26153218