Human genes for hemochromatosis type 4
Hemochromatosis type 4 [DOID:0111028]
A hemochromatosis that has_material_basis_in heterozygous mutation in the SLC40A1 gene on chromosome 2q32.
Synonyms: hemochromatosis type 4, DOID:0111028, autosomal dominant hereditary hemochromatosis, ferroportin disease, hemochromatosis due to defect in ferroportin ...