{"orpha":309845,"name":"Disorder of zinc 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-309845/","orphanet_url":"https://www.orpha.net/en/disease/detail/309845","names":{"fr":{"name":"Anomalie du métabolisme et du transport du zinc"},"de":{"name":"Zink-Stoffwechselstörung"},"es":{"name":"Trastornos del metabolismo del cinc"},"it":{"name":"Difetto del metabolismo dello zinco"},"nl":{"name":"Stoornis van zinkmetabolisme"},"pt":{"name":"Alteração do metabolismo do zinco"},"pl":{"name":"Zaburzenia metabolizmu cynku"},"cs":{"name":"Poruchy metabolismu zinku"},"uk":{"name":"Порушення метаболізму та транспорту цинку"},"zh":{"name":"锌代谢与转运障碍"},"tr":{"name":"Çinko metabolizması ve taşınım bozuklukluğu"}},"xrefs":[{"source":"ICD-10","code":"E83.2","qualifier":"E","icd_relation":"specific","validated":true},{"source":"MONDO","code":"0017764","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"17764","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0268085","qualifier":"E","icd_relation":null,"validated":true},{"source":"MedDRA","code":"10086140","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":37,"name":"Acrodermatitis enteropathica","type":"Disease"},{"orpha":251523,"name":"Hyperzincemia and hypercalprotectinemia","type":"Disease"},{"orpha":505242,"name":"Psychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}