{"orpha":2729,"name":"Okamoto 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 Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome","url":"https://raremap.alftech.space/d/ORPHA-2729/","orphanet_url":"https://www.orpha.net/en/disease/detail/2729","names":{"fr":{"name":"Syndrome d'Okamoto"},"de":{"name":"Okamoto-Syndrom"},"es":{"name":"Síndrome de Okamoto"},"it":{"name":"Sindrome di Okamoto"},"nl":{"name":"Syndroom van Okamoto"},"pt":{"name":"Síndrome Okamuto"},"pl":{"name":"Zespół Okamoto"},"cs":{"name":"Okamotův syndrom"},"uk":{"name":"Синдром Окамото"},"zh":{"name":"Okamoto综合征"},"tr":{"name":"Okamoto sendromu"}},"xrefs":[{"source":"MeSH","code":"C565736","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"4064","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":453499,"name":"Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}