{"orpha":3106,"name":"Robinow-Sorauf 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 Saethre-Chotzen syndrome","url":"https://raremap.alftech.space/d/ORPHA-3106/","orphanet_url":"https://www.orpha.net/en/disease/detail/3106","names":{"fr":{"name":"Syndrome de Robinow-Sorauf"},"de":{"name":"Robinow-Sorauf-Syndrom"},"es":{"name":"Síndrome de Robinow-Sorauf"},"it":{"name":"Sindrome di Robinow-Sorauf"},"nl":{"name":"Syndroom van Robinow-Sorauf"},"pt":{"name":"Síndrome Robinow-Sorauf"},"pl":{"name":"Zespół Robinowa i Soraufa"},"cs":{"name":"Robinowův-Soraufův syndrom","synonyms":["Robinow-Soraufův syndrom"]},"uk":{"name":"Синдром Робінова-Сорауфа"},"zh":{"name":"Robinow-Sorauf综合征"},"tr":{"name":"Robinow-Sorauf sendromu"}},"xrefs":[{"source":"OMIM","code":"180750","qualifier":"E","icd_relation":null,"validated":true},{"source":"MeSH","code":"C537183","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C1867146","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":794,"name":"Saethre-Chotzen syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}