{"orpha":309810,"name":"Disorder of peroxisomal alpha-, beta- and omega-oxidation","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-309810/","orphanet_url":"https://www.orpha.net/en/disease/detail/309810","names":{"fr":{"name":"Anomalie de l'alpha-, bêta- et oméga-oxydation peroxysomales"},"de":{"name":"Störung der peroxisomalen Alpha-, Beta- und Omegaoxidation"},"es":{"name":"Trastornos de la alfa-, beta- y omega- oxidación peroxisomal"},"it":{"name":"Difetto di alfa-, beta- e omega-ossidazione"},"nl":{"name":"Stoornis van peroxisomale alfa-, bèta- en omega-oxidatie"},"pt":{"name":"Alteração da oxidação peroxissomal alfa, beta e ómega"},"pl":{"name":"Zaburzenia peroksymalnej alfa-, beta- i omega- oksydacji"},"cs":{"name":"Poruchy peroxisomální alfa-, beta- a omega-oxidace"},"uk":{"name":"Порушення пероксисомного альфа-, бета- та омега-окислення"},"zh":{"name":"α-，β-，ω-过氧化物酶氧化紊乱"},"tr":{"name":"Peroksizomal alfa, beta ve omega-oksidasyon bozukluğu"}},"xrefs":[{"source":"ICD-11","code":"5C57.1","qualifier":"E","icd_relation":"specific","validated":true,"icd11_uri":"1092479335"},{"source":"MONDO","code":"17753","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681040","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"12476","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":68367,"name":"Rare inborn error of metabolism"},"parents":[{"orpha":68373,"name":"Peroxisomal disease","classifications":[150,156]},{"orpha":506219,"name":"Rare disorder potentially indicated for hematopoietic stem cell transplant","classifications":[233]}],"children":[{"orpha":926,"name":"Acatalasemia","type":"Disease"},{"orpha":773,"name":"Adult Refsum disease","type":"Disease"},{"orpha":79095,"name":"Congenital bile acid synthesis defect type 4","type":"Disease"},{"orpha":35706,"name":"Glutaric acidemia type 3","type":"Disease"},{"orpha":79188,"name":"Peroxisomal beta-oxidation disorder","type":"Category"},{"orpha":93598,"name":"Primary hyperoxaluria type 1","type":"Clinical subtype"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}