{"orpha":254834,"name":"Mitochondrial protein import disorder","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-254834/","orphanet_url":"https://www.orpha.net/en/disease/detail/254834","names":{"fr":{"name":"Anomalie d'import des protéines mitochondriales"},"de":{"name":"Störungen der mitochondrialen Proteinimports"},"es":{"name":"Trastorno de la importación de proteínas mitocondriales"},"it":{"name":"Difetto dell'importo delle proteine mitocondriali"},"nl":{"name":"Stoornis van mitochondriale eiwitimport"},"pt":{"name":"Doença da importação protéica mitocondrial"},"pl":{"name":"Zaburzenie mitochondrialnego importu białek"},"cs":{"name":"Porucha proteinového importu mitochondrií"},"uk":{"name":"Порушення імпорту мітохондріального білка"},"zh":{"name":"线粒体蛋白质转入障碍"},"tr":{"name":"Mitokondriyal protein import bozukluğu"}},"xrefs":[{"source":"ICD-11","code":"5C53.31","qualifier":"E","icd_relation":"specific","validated":true,"icd11_uri":"112110122"},{"source":"MONDO","code":"0016802","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"16802","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680717","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":68367,"name":"Rare inborn error of metabolism"},"parents":[{"orpha":254827,"name":"Mitochondrial membrane transport disorder","classifications":[150,156]}],"children":[{"orpha":52368,"name":"Mohr-Tranebjaerg syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}