A hemochromatosis that has_material_basis_in heterozygous mutation in the FTH1 gene on chromosome 11q12. [ url:https://www.ncbi.nlm.nih.gov/pubmed/11389486 http://purl.obolibrary.org/obo/ECO_0007645 ]
Synonyms: FTH1-associated iron overload FTH1-related iron overload HFE5