{"orpha":54238,"name":"Myotonic dystrophy type 3","type":"Disease","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":[],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Inclusion body myopathy with Paget disease of bone and frontotemporal dementia","url":"https://raremap.alftech.space/d/ORPHA-54238/","orphanet_url":"https://www.orpha.net/en/disease/detail/54238","names":{"fr":{"name":"Dystrophie myotonique type 3"},"de":{"name":"Myotone Dystrophie Typ 3"},"es":{"name":"Distrofia miotónica tipo 3"},"it":{"name":"Distrofia miotonica, tipo 3"},"nl":{"name":"Myotonische dystrofie type 3"},"pt":{"name":"Distrofia miotónica tipo 3"},"pl":{"name":"Dystrofia miotoniczna typu 3"},"cs":{"name":"Myotonická dystrofie, typ 3"},"uk":{"name":"Міотонічна дистрофія, тип 3"},"zh":{"name":"强直性肌营养不良3型"},"tr":{"name":"Miyotonik distrofi tip 3"}},"xrefs":[],"associations":[{"type":"Moved to","orpha":52430,"name":"Inclusion body myopathy with Paget disease of bone and frontotemporal dementia"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}