{"orpha":139491,"name":"OBSOLETE: Hemochromatosis type 4","type":"Disease","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: Autosomal dominant hereditary hemochromatosis","OBSOLETE: Ferroportin disease","OBSOLETE: Hemochromatosis due to defect in ferroportin"],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using SLC40A1-related hemochromatosis","url":"https://raremap.alftech.space/d/ORPHA-139491/","orphanet_url":"https://www.orpha.net/en/disease/detail/139491","names":{"fr":{"name":"OBSOLETE : Hémochromatose type 4","synonyms":["OBSOLETE : Hémochromatose héréditaire autosomique dominante","OBSOLETE : Hémochromatose par défaut en ferroportine","OBSOLETE : Maladie ferroportine"]},"de":{"name":"OBSOLET: Hämochromatose Typ 4","synonyms":["OBSOLET: Hämochromatose durch Ferroportin-Defekt","OBSOLET: Hämochromatose, autosomal-dominante","OBSOLET: Ferroportin-Krankheit"]},"es":{"name":"OBSOLETO: Hemocromatosis tipo 4","synonyms":["OBSOLETO: Enfermedad de la ferroportina","OBSOLETO: Hemocromatosis hereditaria autosómica dominante","OBSOLETO: Hemocromatosis por un defecto de la ferroportina"]},"it":{"name":"OBSOLETO: Emocromatosi, tipo 4","synonyms":["OBSOLETO: Emocromatosi da deficit di ferroportina","OBSOLETO: Emocromatosi ereditaria autosomica dominante","OBSOLETO: Malattia da ferroportina"]},"nl":{"name":"OBSOLEET: Hemochromatose type 4","synonyms":["OBSOLEET: Autosomaal dominante erfelijke hemochromatose","OBSOLEET: Ferroportine-ziekte","OBSOLEET: Hemochromatose door defect van ferroportine"]},"pt":{"name":"OBSOLETO: Doença da ferroportina"},"pl":{"name":"NIEAKTUALNE: Hemochromatoza typu 4","synonyms":["NIEAKTUALNE: Autosomalna dominująca hemochromatoza dziedziczna","NIEAKTUALNE: Choroba ferroportyny","NIEAKTUALNE: Hemochromatoza z powodu defektu ferroportyny"]},"cs":{"name":"NEAKTUÁLNÍ: Hemochromatóza, typ 4","synonyms":["NEAKTUÁLNÍ: Autozomálně dominantní dědičná hemochromatóza","NEAKTUÁLNÍ: Onemocnění ferroportinu","NEAKTUÁLNÍ: Hemochromatóza způsobená poruchou ve ferroportinu"]},"uk":{"name":"ЗАСТАРІЛО: Гемохроматоз, тип 4","synonyms":["ЗАСТАРІЛО: Аутосомно-домінантний спадковий гемохроматоз","ЗАСТАРІЛО: Ферропортиновий синдром","ЗАСТАРІЛО: Гемохроматоз внаслідок дефекту феропортину"]},"zh":{"name":"血色病4型","synonyms":["常染色体显性遗传血色素沉着症"],"definition":"血色素沉着症4型（又称铁转运蛋白病）是一种罕见的遗传性血色素沉着症（HH，见该词条），是一组以遗传性组织铁沉积过多为特征的疾病。"},"tr":{"name":"Hemokromatoz tip 4","synonyms":["Ferroportin hastalığı","Ferroportin defektine bağlı hemokromatoz","Otozomal dominant kalıtsal hemokromatoz"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":647834,"name":"SLC40A1-related hemochromatosis"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}