{"orpha":3046,"name":"OBSOLETE: Intellectual disability-unusual facies, Davis-Lafer type","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: Davis-Lafer 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-3046/","orphanet_url":"https://www.orpha.net/en/disease/detail/3046","names":{"fr":{"name":"OBSOLETE : Syndrome de déficience intellectuelle-facis anormal, type Davis-Lafer","synonyms":["OBSOLETE : Syndrome de Davis-Lafer"]},"de":{"name":"OBSOLET: Intelligenzminderung mit Gesichtsanomalien Typ Davis-Lafer","synonyms":["OBSOLET: Davis-Lafer-Syndrom"]},"es":{"name":"OBSOLETO: Discapacidad intelectual-facies inusual tipo Davis-Lafer","synonyms":["OBSOLETO: Síndrome de Davis-Lafer"]},"it":{"name":"OBSOLETO: Disabilità intellettiva-anomalie facciali, tipo Davis Lafer","synonyms":["OBSOLETO: Sindrome di Davis-Lafer"]},"nl":{"name":"OBSOLEET: Intellectuele achterstand - ongewoon uiterlijk, Davis-Lafer-type","synonyms":["OBSOLEET: Davis-Lafersyndroom"]},"pt":{"name":"OBSOLETO: Perturbação do desenvolvimento intelectual-face peculiar, tipo Davis-Lafer","synonyms":["OBSOLETO: Síndrome Davis-Lafer"]},"pl":{"name":"NIEAKTUALNE: Niepelnosprawnosc intelektualna - niezwykla twarz typu Davisa i Lafera","synonyms":["NIEAKTUALNE: Zespół Davisa i Lafera"]},"cs":{"name":"NEAKTUÁLNÍ: Mentální retardaci a neobvyklá tvář, typ Davis-Lafer","synonyms":["OBSOLETE: Davis-Lafer syndrome"]},"uk":{"name":"ЗАСТАРІЛО: Розумова відсталість - незвичайні риси обличчя, тип Девіса-Лафера","synonyms":["ЗАСТАРІЛО: Синдром Девіса-Лафера"]},"zh":{"name":"弃用：智力障碍-异常面容综合征， Davis-Lafer亚型","synonyms":["Davis-Lafer综合征"]},"tr":{"name":"Eski adı: Zihinsel yetersizlik-alışılmadık yüz, Davis-Lafer tipi","synonyms":["Davis-Lafer 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}