{"orpha":1611,"name":"OBSOLETE: Deletion 20p","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: Monosomy 20p"],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Partial deletion of the short arm of chromosome 20","url":"https://raremap.alftech.space/d/ORPHA-1611/","orphanet_url":"https://www.orpha.net/en/disease/detail/1611","names":{"fr":{"name":"OBSOLETE : Délétion 20p","synonyms":["OBSOLETE : Monosomie 20p"]},"de":{"name":"OBSOLET: Deletion 20p","synonyms":["OBSOLET: Monosomie 20p"]},"es":{"name":"OBSOLETO: Deleción 20p","synonyms":["OBSOLETO: Monosomía 20p"]},"it":{"name":"OBSOLETO: Delezione 20p","synonyms":["OBSOLETO: Monosomia 20p"]},"nl":{"name":"OBSOLEET: Deletie 20p","synonyms":["OBSOLEET: Monosomie 20p"]},"pt":{"name":"OBSOLETO: Deleção 20p","synonyms":["OBSOLETO: Monossomia 20p"]},"pl":{"name":"NIEAKTUALNE: Delecja 20p","synonyms":["NIEAKTUALNE: Monosomia 20p"]},"cs":{"name":"NEAKTUÁLNÍ: Deletion 20p","synonyms":["OBSOLETE: Monosomy 20p"]},"uk":{"name":"ЗАСТАРІЛО: Делеція 20p","synonyms":["ЗАСТАРІЛО: Моносомія 20р"]},"zh":{"name":"弃用：20号染色体短臂缺失","synonyms":["20号染色体短臂单体"]},"tr":{"name":"Eski adı: Delesyon 20p","synonyms":["Monozomi 20p"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":261992,"name":"Partial deletion of the short arm of chromosome 20 syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}