Human genes for hemochromatosis type 3
Hemochromatosis type 3 [DOID:0111030]
A hemochromatosis that has_material_basis_in homozygous or compound heterozygous mutation in the TFR2 gene on chromosome 7q22.
Synonyms: hemochromatosis type 3, DOID:0111030, hemochromatosis due to defect in transferrin receptor 2, HFE3, TFR2-related hemochromatosis ...