{"orpha":207006,"name":"OBSOLETE: Acquired amyloid myopathy","type":"Category","group":"Group of disorders","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Acquired skeletal muscle disease","url":"https://raremap.alftech.space/d/ORPHA-207006/","orphanet_url":"https://www.orpha.net/en/disease/detail/207006","names":{"fr":{"name":"OBSOLETE : Myopathie amyloïde acquise"},"de":{"name":"OBSOLET: Amyloidmyopathie, erworbene"},"es":{"name":"OBSOLETO: Miopatía amiloide adquirida"},"it":{"name":"OBSOLETO: Miopatia amiloide acquisita"},"nl":{"name":"OBSOLEET: Verworven amyloïde myopathie"},"pt":{"name":"OBSOLETO: Miopatia amilóide adquirida"},"pl":{"name":"NIEAKTUALNE: Nabyta miopatia amyloidowa"},"cs":{"name":"NEAKTUÁLNÍ: Získaná amyloidová myopatie"},"uk":{"name":"ЗАСТАРІЛО: Набута амілоїдна міопатія"},"zh":{"name":"弃用：获得性淀粉样肌病"},"tr":{"name":"Eski adı: Edinsel amiloid miyopati"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":206638,"name":"Acquired skeletal muscle disease"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}