{"orpha":309824,"name":"Disorder of metabolite absorption 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-309824/","orphanet_url":"https://www.orpha.net/en/disease/detail/309824","names":{"fr":{"name":"Anomalie de transport et d'absorption des métabolites"},"de":{"name":"Metabolitenstoffwechsel- und Transportstörungen"},"es":{"name":"Trastornos de absorción y transporte de metabolitos"},"it":{"name":"Difetto del trasporto e dell'assorbimento dei metaboliti"},"nl":{"name":"Stoornis van metabolietabsorptie en transport"},"pt":{"name":"Alteração da absorção e transporte de metabólitos"},"pl":{"name":"Zaburzenia wchłaniania i transportu metabolitów"},"cs":{"name":"Poruchy absorpce a transportu metabolitů"},"uk":{"name":"Порушення всмоктування та транспорту метаболітів"},"zh":{"name":"代谢物吸收-转运障碍"},"tr":{"name":"Metabolit emilim ve taşınım bozuklukluğu"}},"xrefs":[{"source":"MONDO","code":"0017757","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"17757","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681033","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":68367,"name":"Rare inborn error of metabolism"},"parents":[{"orpha":68367,"name":"Rare inborn error of metabolism","classifications":[150,156]}],"children":[{"orpha":309836,"name":"Disorder of mineral absorption and transport","type":"Category"},{"orpha":309827,"name":"Disorder of vitamin and non-protein cofactor absorption and transport","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}