{"orpha":309120,"name":"Acyl-CoA dehydrogenase deficiency","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-309120/","orphanet_url":"https://www.orpha.net/en/disease/detail/309120","names":{"fr":{"name":"Déficit en acyl-CoA déshydrogénase"},"de":{"name":"Acyl-CoA-Dehydrogenase-Mangel"},"es":{"name":"Deficiencia de acil-CoA deshidrogenasa"},"it":{"name":"Deficit di acil-CoA deidrogenasi"},"nl":{"name":"Acyl-CoA-dehydrogenasedeficiëntie"},"pt":{"name":"Défice de acil-CoA desidrogenase"},"pl":{"name":"Niedobór dehydrogenazy acylo-CoA"},"cs":{"name":"Deficit acyl-CoA-dehydrogenázy"},"uk":{"name":"Дефіцит ацил-КоА-дегідрогенази"},"zh":{"name":"酰基辅酶A脱氢酶缺乏症"},"tr":{"name":"Açil-KoA dehidrojenaz eksikliği"}},"xrefs":[{"source":"MONDO","code":"0017714","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"17714","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0268635","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":68367,"name":"Rare inborn error of metabolism"},"parents":[{"orpha":309115,"name":"Disorder of fatty acid oxidation and ketogenesis","classifications":[150,156]}],"children":[{"orpha":42,"name":"Medium chain acyl-CoA dehydrogenase deficiency","type":"Disease"},{"orpha":26791,"name":"Multiple acyl-CoA dehydrogenase deficiency","type":"Disease"},{"orpha":26792,"name":"Short chain acyl-CoA dehydrogenase deficiency","type":"Disease"},{"orpha":329942,"name":"Transient neonatal multiple acyl-CoA dehydrogenase deficiency","type":"Disease"},{"orpha":26793,"name":"Very long chain acyl-CoA dehydrogenase deficiency","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}