hemochromatosis type 4

hemochromatosis type 4

an autosomal dominant disorder [MIM*606069] caused by a mutation in the gene SLC11A3, which encodes ferroportin on 2q32.
References in periodicals archive ?
3 Hemochromatosis Type 2 Type 2A HJV Hemojuvelin 1q21 Type 2B HAMP Hepcidin 19q13 Hemochromatosis Type 3 TFR2 Transferrin receptor 2 7q22 Hemochromatosis Type 4 SLC40A1 Ferroportin 2q32 Disorder Treatment Hemochromatosis Type 1 Phlebotomy, iron chelating therapy Hemochromatosis Type 2 Phlebotomy, iron chelating therapy Type 2A Type 2B Hemochromatosis Type 3 Phlebotomy, iron chelating therapy Hemochromatosis Type 4 Phlebotomy, erythropoietin