{"orpha":2507,"name":"OBSOLETE: Mickleson syndrome","type":"Malformation syndrome","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 Primary bone dysplasia","url":"https://raremap.alftech.space/d/ORPHA-2507/","orphanet_url":"https://www.orpha.net/en/disease/detail/2507","names":{"fr":{"name":"OBSOLETE : Syndrome de Mickleson"},"de":{"name":"OBSOLET: Mickleson-Syndrom"},"es":{"name":"OBSOLETO: Síndrome de Mickleson"},"it":{"name":"OBSOLETO: Sindrome di Mickleson"},"nl":{"name":"OBSOLEET: Syndroom van Mickleson"},"pt":{"name":"OBSOLETO: Síndrome Mickleson"},"pl":{"name":"NIEAKTUALNE: Zespól Micklesona"},"cs":{"name":"NEAKTUÁLNÍ: Micklesonův syndrome"},"uk":{"name":"ЗАСТАРІЛО: Синдром Міклесона"},"zh":{"name":"弃用：Mickleson综合征"},"tr":{"name":"Eski adı: Mickleson sendromu"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":364526,"name":"Primary bone dysplasia"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}