{"orpha":300763,"name":"Laminopathy with lipodystrophy","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-300763/","orphanet_url":"https://www.orpha.net/en/disease/detail/300763","names":{"fr":{"name":"Laminopathie avec lipodystrophie"},"de":{"name":"Laminopathie mit Lipodystrophie"},"es":{"name":"Laminopatía con lipodistrofia"},"it":{"name":"Laminopatia con lipodistrofia"},"nl":{"name":"Laminopathie met lipodystrofie"},"pt":{"name":"Laminopatia com lipodistrofia"},"pl":{"name":"Laminopatia z lipodystrofią"},"cs":{"name":"Laminopatie s lipodystrofií"},"uk":{"name":"Ламінопатія з ліподистрофією"},"zh":{"name":"核纤层蛋白病伴脂肪萎缩综合征"},"tr":{"name":"Lipodistrofi ile seyreden laminopati"}},"xrefs":[{"source":"UMLS","code":"C5681084","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97978,"name":"Rare endocrine disease"},"parents":[{"orpha":98301,"name":"Laminopathy","classifications":[156]}],"children":[{"orpha":280365,"name":"Autosomal semi-dominant severe lipodystrophic laminopathy","type":"Disease"},{"orpha":2348,"name":"Familial partial lipodystrophy, Dunnigan type","type":"Disease"},{"orpha":79084,"name":"Familial partial lipodystrophy, Köbberling type","type":"Disease"},{"orpha":90153,"name":"Mandibuloacral dysplasia with type A lipodystrophy","type":"Clinical subtype"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[{"type":"Point prevalence","qualification":"Class only","class":"Unknown","value":0.0,"area":"Worldwide","status":"Not yet validated","source":"ORPHANET"}],"phenotypes":null}