{"orpha":254837,"name":"Unspecified mitochondrial disorder","type":"Clinical group","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-254837/","orphanet_url":"https://www.orpha.net/en/disease/detail/254837","names":{"fr":{"name":"Anomalie mitochondriale non spécifiée"},"de":{"name":"Mitochondriale Krankheit, unspezifische"},"es":{"name":"Trastorno mitocondrial no especificado"},"it":{"name":"Anomalia mitocondriale non specificata"},"nl":{"name":"Niet-gespecificeerde mitochondriale stoornis"},"pt":{"name":"Doença mitocondrial não específica"},"pl":{"name":"Niespecyficzne zaburzenie mitochondrialne"},"cs":{"name":"Nespecifická porucha mitochondrií"},"uk":{"name":"Невизначений мітохондріальний розлад"},"zh":{"name":"未指明的线粒体疾病"},"tr":{"name":"Tanısız mitokondriyal bozukluk"}},"xrefs":[{"source":"MONDO","code":"16803","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680715","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":656279,"name":"1p36.33 duplication syndrome","type":"Disease"},{"orpha":98672,"name":"Autosomal dominant optic atrophy","type":"Clinical group"},{"orpha":51188,"name":"Ethylmalonic encephalopathy","type":"Disease"},{"orpha":137675,"name":"Histiocytoid cardiomyopathy","type":"Disease"},{"orpha":502423,"name":"Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome","type":"Disease"},{"orpha":2597,"name":"Mitochondrial myopathy-lactic acidosis-deafness syndrome","type":"Disease"},{"orpha":496790,"name":"Ocular anomalies-axonal neuropathy-developmental delay syndrome","type":"Disease"},{"orpha":2802,"name":"X-linked sideroblastic anemia and spinocerebellar ataxia","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":["Autosomal recessive","X-linked recessive"],"onset":[],"prevalence":[],"phenotypes":null}