{"orpha":309851,"name":"Disorder of manganese 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-309851/","orphanet_url":"https://www.orpha.net/en/disease/detail/309851","names":{"fr":{"name":"Anomalie du transport du manganèse"},"de":{"name":"Mangantransport-Störung"},"es":{"name":"Trastornos de transporte del manganeso"},"it":{"name":"Difetto del trasporto del manganese"},"nl":{"name":"Stoornis van mangaantransport"},"pt":{"name":"Alteração do transporte de manganésio"},"pl":{"name":"Zaburzenia transportu manganu"},"cs":{"name":"Poruchy metabolismu manganu"},"uk":{"name":"Порушення транспорту марганцю"},"zh":{"name":"锰迁移障碍"},"tr":{"name":"Manganez taşınım bozuklukluğu"}},"xrefs":[{"source":"MONDO","code":"0017766","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"17766","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681032","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":309854,"name":"Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome","type":"Disease"},{"orpha":521406,"name":"Dystonia-parkinsonism-hypermanganesemia syndrome","type":"Disease"},{"orpha":468699,"name":"SLC39A8-CDG","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}