{"orpha":309028,"name":"Disorder of lipid absorption and transport","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-309028/","orphanet_url":"https://www.orpha.net/en/disease/detail/309028","names":{"fr":{"name":"Trouble du transport et de l'absorption des lipides"},"de":{"name":"Fettstoffwechsel-Störung"},"es":{"name":"Trastornos de absorción y transporte de lípidos"},"it":{"name":"Difetto dell'assorbimento e del trasporto dei lipidi"},"nl":{"name":"Stoornis van lipidenabsorptie en transport"},"pt":{"name":"Alteração da absorção lipídica e transporte"},"pl":{"name":"Zaburzenia wchłaniania i transportu lipidów"},"cs":{"name":"Poruchy absorpce a transportu lipidů"},"uk":{"name":"Порушення всмоктування та транспортування ліпідів"},"zh":{"name":"脂质吸收-转运障碍"},"tr":{"name":"Lipid emilimi ve taşınması bozukluğu"}},"xrefs":[{"source":"ICD-11","code":"5C62","qualifier":"E","icd_relation":"specific","validated":true,"icd11_uri":"1858691234"},{"source":"MONDO","code":"17709","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681072","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":68367,"name":"Rare inborn error of metabolism"},"parents":[{"orpha":309005,"name":"Disorder of lipid metabolism","classifications":[150,156]},{"orpha":165661,"name":"Genetic pancreatic disease","classifications":[156]},{"orpha":101937,"name":"Rare pancreatic disease","classifications":[152]}],"children":[{"orpha":309111,"name":"Combined pancreatic lipase-colipase deficiency","type":"Disease"},{"orpha":309108,"name":"Pancreatic colipase deficiency","type":"Disease"},{"orpha":309031,"name":"Pancreatic triacylglycerol lipase deficiency","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}