{"orpha":300766,"name":"Laminopathy with premature aging","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-300766/","orphanet_url":"https://www.orpha.net/en/disease/detail/300766","names":{"fr":{"name":"Laminopathie avec vieillissement prématuré"},"de":{"name":"Laminopathie mit vorzeitiger Alterung"},"es":{"name":"Laminopatía con envejecimiento prematuro"},"it":{"name":"Laminopatia con invecchiamento precoce"},"nl":{"name":"Laminopathie met vroegtijdige veroudering"},"pt":{"name":"Laminopatia com envelhecimento prematuro"},"pl":{"name":"Laminopatia z przedwczesnym starzeniem"},"cs":{"name":"Laminopatie s předčasným stárnutím"},"uk":{"name":"Ламінопатія з передчасним старінням"},"zh":{"name":"核纤层蛋白病伴早衰"},"tr":{"name":"Erken yaşlanma ile seyreden laminopati"}},"xrefs":[{"source":"UMLS","code":"C5567864","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":99706,"name":"OBSOLETE: Progeria-associated arthropathy","status":"inactive"}],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":98301,"name":"Laminopathy","classifications":[156]}],"children":[{"orpha":79474,"name":"Atypical Werner syndrome","type":"Disease"},{"orpha":740,"name":"Hutchinson-Gilford progeria syndrome","type":"Disease"},{"orpha":363618,"name":"LMNA-related cardiocutaneous progeria syndrome","type":"Disease"},{"orpha":1662,"name":"Restrictive dermopathy","type":"Disease"}],"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}