{"orpha":309842,"name":"Disorder of iron metabolism and transport","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"definition":null,"note":"This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.","url":"https://raremap.alftech.space/d/ORPHA-309842/","orphanet_url":"https://www.orpha.net/en/disease/detail/309842","names":{"fr":{"name":"Anomalie du transport et du métabolisme du fer"},"de":{"name":"Eisen-Stoffwechsel- und Transportstörungen"},"es":{"name":"Trastornos del metabolismo y del transporte del hierro"},"it":{"name":"Difetto del trasporto e del metabolismo del ferro"},"nl":{"name":"Stoornis van ijzermetabolisme en transport"},"pt":{"name":"Alteração do metabolismo e transporte de ferro"},"pl":{"name":"Zaburzenia metabolizmu i transportu żelaza"},"cs":{"name":"Poruchy metabolismu a transportu železa"},"uk":{"name":"Порушення метаболізму та транспорту заліза"},"zh":{"name":"铁代谢和转运障碍"},"tr":{"name":"Demir metabolizması ve taşınım bozuklukluğu"}},"xrefs":[{"source":"ICD-10","code":"E83.1","qualifier":"E","icd_relation":"specific","validated":true},{"source":"MONDO","code":"0017763","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"17763","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681031","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":68367,"name":"Rare inborn error of metabolism"},"parents":[{"orpha":309836,"name":"Disorder of mineral absorption and transport","classifications":[150,156]}],"children":[{"orpha":48818,"name":"Aceruloplasminemia","type":"Disease"},{"orpha":1195,"name":"Congenital atransferrinemia","type":"Disease"},{"orpha":139507,"name":"Dietary iron overload disease","type":"Disease"},{"orpha":247790,"name":"FTH1-related iron overload","type":"Disease"},{"orpha":648562,"name":"Ferroportin disease","type":"Disease"},{"orpha":163,"name":"Hereditary hyperferritinemia-cataract syndrome","type":"Disease"},{"orpha":440731,"name":"L-ferritin deficiency","type":"Biological anomaly"},{"orpha":83642,"name":"Microcytic anemia with liver iron overload","type":"Disease"},{"orpha":446,"name":"Neonatal hemochromatosis","type":"Disease"},{"orpha":157846,"name":"Neuroferritinopathy","type":"Disease"},{"orpha":727296,"name":"Progressive muscle weakness-respiratory insufficiency-learning difficulty syndrome","type":"Disease"},{"orpha":220489,"name":"Rare hereditary hemochromatosis","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}