{"orpha":79188,"name":"Peroxisomal beta-oxidation 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-79188/","orphanet_url":"https://www.orpha.net/en/disease/detail/79188","names":{"fr":{"name":"Anomalie de la bêta-oxydation péroxysomale"},"de":{"name":"Peroxisomale beta-Oxidationsstörung"},"es":{"name":"Enfermedad de la beta oxidación peroxisomal"},"it":{"name":"Malattia della beta-ossidazione perossisomiale"},"nl":{"name":"Stoornis van peroxisomale bèta-oxidatie"},"pt":{"name":"Doença da beta-oxidação peroxissomal"},"pl":{"name":"Zaburzenie beta-oksydacji peroksysomalnej"},"cs":{"name":"Porucha peroxisomální beta oxidace"},"uk":{"name":"Порушення пероксисомного бета-окислення"},"zh":{"name":"过氧化物酶体β氧化异常"},"tr":{"name":"Peroksizomal beta oksidasyonu bozukluğu"}},"xrefs":[{"source":"MONDO","code":"0019233","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"19233","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681280","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"12470","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":68367,"name":"Rare inborn error of metabolism"},"parents":[{"orpha":309810,"name":"Disorder of peroxisomal alpha-, beta- and omega-oxidation","classifications":[150,156,233]}],"children":[{"orpha":300,"name":"Bifunctional enzyme deficiency","type":"Disease"},{"orpha":163684,"name":"Leukoencephalopathy-dystonia-motor neuropathy syndrome","type":"Disease"},{"orpha":2971,"name":"Peroxisomal acyl-CoA oxidase deficiency","type":"Disease"},{"orpha":43,"name":"X-linked adrenoleukodystrophy","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}