{"orpha":3118,"name":"Rudiger syndrome","type":"Malformation syndrome","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 Schinzel-Giedion syndrome","url":"https://raremap.alftech.space/d/ORPHA-3118/","orphanet_url":"https://www.orpha.net/en/disease/detail/3118","names":{"fr":{"name":"Syndrome de Rudiger"},"de":{"name":"Rüdiger-Syndrom"},"es":{"name":"Síndrome de Rudiger"},"it":{"name":"Sindrome di Rudiger"},"nl":{"name":"Syndroom van Rudiger"},"pt":{"name":"Síndrome Rudiger"},"pl":{"name":"Zespół Rudigera"},"cs":{"name":"Rudigerův syndrom"},"uk":{"name":"Синдром Рудігера"},"zh":{"name":"Rudiger综合征"},"tr":{"name":"Rudiger sendromu"}},"xrefs":[{"source":"OMIM","code":"268650","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C3502049","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":798,"name":"Schinzel-Giedion syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}