{"orpha":2474,"name":"OBSOLETE: McLain-Dekaban syndrome","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: Intellectual disability-coloboma-slimness syndrome"],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Multiple congenital anomalies/dysmorphic syndrome-intellectual disability","url":"https://raremap.alftech.space/d/ORPHA-2474/","orphanet_url":"https://www.orpha.net/en/disease/detail/2474","names":{"fr":{"name":"OBSOLETE : Syndrome de McLain-Dekaban","synonyms":["OBSOLETE : Déficience intellectuelle-minceur-colobome"]},"de":{"name":"OBSOLET: Mclain-Debakian-Syndrom"},"es":{"name":"OBSOLETO: Síndrome de McLain-Dekaban","synonyms":["OBSOLETO: Síndrome de discapacidad intelectual-coloboma-delgadez"]},"it":{"name":"OBSOLETO: Sindrome di McLain-Debakian","synonyms":["OBSOLETO: Sindrome disabilità intellettiva-coloboma-magrezza"]},"nl":{"name":"OBSOLEET: Syndroom van McLain-Dekaban","synonyms":["OBSOLEET: Intellectuele achterstand - coloboom - slankheid-syndroom"]},"pt":{"name":"OBSOLETO: Síndrome Mclain-Debakian","synonyms":["OBSOLETO: Síndrome de perturbação do desenvolvimento intelectual-coloboma-magreza"]},"pl":{"name":"NIEAKTUALNE: Zespól McLaina i Dekabana","synonyms":["NIEAKTUALNE: Niepełnosprawność intelektualna - coloboma - wątłość"]},"cs":{"name":"NEAKTUÁLNÍ: McLain-Dekabanův syndrom","synonyms":["OBSOLETE: Intellectual disability-coloboma-slimness syndrome"]},"uk":{"name":"ЗАСТАРІЛО: Синдром Маклайна-Декабана","synonyms":["ЗАСТАРІЛО: Синдром інтелектуальної недостатності - колобоми - худорлявості"]},"zh":{"name":"弃用：McLain-Dekaban 综合征","synonyms":["智力障碍-缺损-苗条综合征"]},"tr":{"name":"Eski adı: McLain-Dekaban sendromu","synonyms":["Zihinsel yetersizlik-kolobom-zayıflık sendromu"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":102283,"name":"Multiple congenital anomalies/dysmorphic syndrome-intellectual disability"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}