Term Name:	hemochromatosis type 4
Synonyms:	autosomal dominant hereditary hemochromatosis, ferroportin disease, hemochromatosis due to defect in ferroportin, HFE4
Definition:	A hemochromatosis that has_material_basis_in heterozygous mutation in the SLC40A1 gene on chromosome 2q32.
Ontology:	Human Disease [DOID:0111028]   ( DOID:0111028 )