{"orpha":254827,"name":"Mitochondrial membrane transport 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-254827/","orphanet_url":"https://www.orpha.net/en/disease/detail/254827","names":{"fr":{"name":"Anomalie de transport membranaire mitochondrial"},"de":{"name":"Mitochondriale Membrantransportstörung"},"es":{"name":"Trastorno en el transporte de la membrana mitocondrial"},"it":{"name":"Difetto del trasporto nelle membrane mitocondriali"},"nl":{"name":"Stoornis van mitochondriaal membraantransport"},"pt":{"name":"Doença do transporte membranar mitocondrial"},"pl":{"name":"Zaburzenie transportu przez błonę mitochondrialną"},"cs":{"name":"Porucha transportu mitochondriální membránou"},"uk":{"name":"Порушення мембранного транспорту мітохондрій"},"zh":{"name":"线粒体膜转运障碍"},"tr":{"name":"Mitokondriyal membran taşıma bozukluğu"}},"xrefs":[{"source":"ICD-11","code":"5C53.3","qualifier":"E","icd_relation":"specific","validated":true,"icd11_uri":"1340308055"},{"source":"MONDO","code":"0016800","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"16800","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680718","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":68367,"name":"Rare inborn error of metabolism"},"parents":[{"orpha":68380,"name":"Mitochondrial disease","classifications":[150,156]}],"children":[{"orpha":254834,"name":"Mitochondrial protein import disorder","type":"Category"},{"orpha":254830,"name":"Mitochondrial substrate carrier disorder","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}