{"orpha":308451,"name":"Disorder of neutral amino acid 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-308451/","orphanet_url":"https://www.orpha.net/en/disease/detail/308451","names":{"fr":{"name":"Trouble du transport des acides aminés neutres"},"de":{"name":"Transportstörung neutraler Aminosäuren"},"es":{"name":"Trastornos del transporte de aminoácidos neutros"},"it":{"name":"Difetto del trasporto degli amminoacidi neutri"},"nl":{"name":"Stoornis van transport van neutrale aminozuren"},"pt":{"name":"Alteração do transporte de aminoácidos neutros"},"pl":{"name":"Zaburzenie transportu neutralnych aminokwasów"},"cs":{"name":"Poruchy transportu neutrálních aminokyselin"},"uk":{"name":"Порушення транспорту нейтральних амінокислот"},"zh":{"name":"中性氨基酸转移紊乱"},"tr":{"name":"Nötral amino asit taşınması bozukluğu"}},"xrefs":[{"source":"MONDO","code":"0017687","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"17687","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5848149","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":68367,"name":"Rare inborn error of metabolism"},"parents":[{"orpha":79166,"name":"Disorder of amino acid absorption and transport","classifications":[150,156]}],"children":[{"orpha":2116,"name":"Hartnup disease","type":"Disease"},{"orpha":42062,"name":"Iminoglycinuria","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}