{"orpha":3276,"name":"Disorder of plasmalogens biosynthesis","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-3276/","orphanet_url":"https://www.orpha.net/en/disease/detail/3276","names":{"fr":{"name":"Anomalie de la biosynthèse des plasmalogènes"},"de":{"name":"Plasmalogenbiosynthesedefekt"},"es":{"name":"Trastorno de la biosíntesis de plasmalógenos"},"it":{"name":"Difetto della biosintesi dei plasmalogeni"},"nl":{"name":"Stoornis van plasmalogeenbiosynthese"},"pt":{"name":"Doença da biossíntese dos plasmalogéneos"},"pl":{"name":"Zaburzenia biosyntezy plazmalogenu"},"cs":{"name":"Porucha biosyntézy plasmalogenů"},"uk":{"name":"Порушення біосинтезу плазмогенів"},"zh":{"name":"缩醛磷脂生物合成紊乱"},"tr":{"name":"Plazmalojen biyosentez bozukluğu"}},"xrefs":[{"source":"MONDO","code":"0017986","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"17986","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681192","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]}],"children":[{"orpha":438178,"name":"Fatty acyl-CoA reductase 1 deficiency","type":"Disease"},{"orpha":177,"name":"Rhizomelic chondrodysplasia punctata","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}