{"orpha":79204,"name":"Lipid storage disease","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-79204/","orphanet_url":"https://www.orpha.net/en/disease/detail/79204","names":{"fr":{"name":"Maladie de surchage lipidique"},"de":{"name":"Lipidspeicherkrankheit"},"es":{"name":"Enfermedad por depósito de lípidos"},"it":{"name":"Malattia da deposito di lipidi"},"nl":{"name":"Vetstapelingsziekte"},"pt":{"name":"Doença de armazenamento lipídico"},"pl":{"name":"Choroba spichrzania tłuszczy"},"cs":{"name":"Lipidózy"},"uk":{"name":"Хвороба накопичення ліпідів"},"zh":{"name":"脂质贮积症"},"tr":{"name":"Lipid depo hastalığı"}},"xrefs":[{"source":"MONDO","code":"19245","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0023794","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":68367,"name":"Rare inborn error of metabolism"},"parents":[{"orpha":79225,"name":"Sphingolipidosis","classifications":[150,156,233]}],"children":[{"orpha":275761,"name":"Lysosomal acid lipase deficiency","type":"Disease"},{"orpha":646,"name":"Niemann-Pick disease type C","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}