{"orpha":3043,"name":"OBSOLETE: Intellectual disability-unusual facies syndrome","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: Morillo Cucci-Passarge syndrome"],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Rare syndromic intellectual disability","url":"https://raremap.alftech.space/d/ORPHA-3043/","orphanet_url":"https://www.orpha.net/en/disease/detail/3043","names":{"fr":{"name":"OBSOLETE : Syndrome de déficience intellectuelle-dysmorphie-hyperlaxité","synonyms":["OBSOLETE : Syndrome de Morillo-Cucci-Passarge"]},"de":{"name":"OBSOLET: Intelligenzminderung-ungewöhnliche Fazies-Syndrom","synonyms":["OBSOLET: Morillo-Cucci-Passarge-Syndrom"]},"es":{"name":"OBSOLETO: Síndrome de discapacidad intelectual-facies inusual","synonyms":["OBSOLETO: Síndrome de Morillo Cucci-Passarge"]},"it":{"name":"OBSOLETO: Sindrome disabilità intellettiva-dismorfismi","synonyms":["OBSOLETO: Sindrome di Morillo-Cucci-Passarge"]},"nl":{"name":"OBSOLEET: Intellectuele achterstand - ongewoon uiterlijk-syndroom","synonyms":["OBSOLEET: Syndroom van Morillo Cucci-Passarge"]},"pt":{"name":"OBSOLETO: Síndrome de perturbação do desenvolvimento intelectual-face peculiar","synonyms":["OBSOLETO: Síndrome Morillo-Cucci-Passarge"]},"pl":{"name":"NIEAKTUALNE: Niepelnosprawnosc intelektualna - niezwykla twarz","synonyms":["NIEAKTUALNE: Zespół Morillo Cucci i Passarge"]},"cs":{"name":"NEAKTUÁLNÍ: Syndrom zahrnující mentální retardaci a neobvyklou tvář","synonyms":["OBSOLETE: Morillo Cucci-Passarge syndrome"]},"uk":{"name":"ЗАСТАРІЛО: Синдром розумової відсталості з незвичайними рисами обличчям","synonyms":["ЗАСТАРІЛО: Синдром Морілло-Куччі-Пассаржа: синдром Морілло-Куччі-Пассаржа"]},"zh":{"name":"弃用：智力障碍-异常面容综合征","synonyms":["Morillo Cucci-Passarge综合征"]},"tr":{"name":"Eski adı: zihinsel yetersizlik-alışılmadık yüz sendromu","synonyms":["Morillo Cucci-Passarge sendromu"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":102369,"name":"Rare syndromic intellectual disability"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}