{"orpha":278,"name":"OBSOLETE: Corticobasal degeneration","type":"Disease","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Corticobasal syndrome","url":"https://raremap.alftech.space/d/ORPHA-278/","orphanet_url":"https://www.orpha.net/en/disease/detail/278","names":{"fr":{"name":"OBSOLETE : Dégénérescence corticobasale"},"de":{"name":"OBSOLET: Degeneration, kortiko-basale"},"es":{"name":"OBSOLETO: Degeneración cortico-basal"},"it":{"name":"OBSOLETO: Degenerazione corticobasale"},"nl":{"name":"OBSOLEET: Corticobasale degeneratie"},"pt":{"name":"OBSOLETO: Degenerescência cortico-basal"},"pl":{"name":"NIEAKTUALNE: Zwyrodnienie korowo-podstawne"},"cs":{"name":"NEAKTUÁLNÍ: Kortikobazální degenerace"},"uk":{"name":"ЗАСТАРІЛО: Кортикобазальна дегенерація"},"zh":{"name":"弃用：皮质基底节变性"},"tr":{"name":"Eski adı: Kortikobazal dejenerasyon"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":454887,"name":"Corticobasal syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}