{"orpha":330197,"name":"OBSOLETE: Genetic multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome","type":"Category","group":"Group of disorders","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: Genetic MCA/variable MR","OBSOLETE: Genetic multiple congenital anomalies-variable intellectual disability with or without dysmorphism syndrome"],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.<br/><br/>Instead, consider using Genetic multiple congenital anomalies/dysmorphic syndrome-intellectual disability","url":"https://raremap.alftech.space/d/ORPHA-330197/","orphanet_url":"https://www.orpha.net/en/disease/detail/330197","names":{"fr":{"name":"OBSOLETE : Anomalies congénitales multiples-déficience intellectuelle variable d'origine génétique","synonyms":["OBSOLETE : MCA/MR variable d'origine génétique"]},"de":{"name":"OBSOLET: Genetisch bedingte multiple kongenitale Anomalien/Dysmorphie-Syndrom mit variabler Intelligenzminderung","synonyms":["OBSOLET: Genetisch bedingte multiple kongenitale Anomalien mit variabler Intelligenzminderung","OBSOLET: Genetisch bedingtes multiples Dysmorphie-Syndrom mit variabler Intelligenzminderung"]},"es":{"name":"OBSOLETO: Síndrome de anomalías congénitas múltiples/síndrome dismórfico-discapacidad intelectual variable de origen genético","synonyms":["OBSOLETO: Síndrome de anomalías congénitas múltiples-discapacidad intelectual variable con o sin dismorfia de origen genético"]},"it":{"name":"OBSOLETO: Sindrome genetica da anomalie/dismorfismi congeniti multipli- sindrome disabilità intellettiva variabile","synonyms":["OBSOLETO: Sindrome genetica da anomalie congenite multiple-disabilità intellettiva variabile con o senza dismorfismi","OBSOLETO: MCA/MR variabile, di origine genetica","OBSOLETO: Sindrome genetica da anomalie congenite multiple e disabilità intellettiva variabile con o senza dismorfismi"]},"nl":{"name":"OBSOLEET: Genetische multipele congenitale anomalieën/dysmorfie-syndroom - variabele intellectuele achterstand-syndroom","synonyms":["OBSOLEET: Genetische MCA/variabele MR","OBSOLEET: Genetische multipele congenitale anomalieën - variabele intellectuele achterstand met of zonder dysmorfie-syndroom"]},"pt":{"name":"OBSOLETO: Síndrome de anomalias congénitas múltiplas genéticas/dismorfias-perturbação do desenvolvimento intelectual variável"},"pl":{"name":"NIEAKTUALNE: Mnogie genetycznie uwarunkowane wady wrodzone/zespół dysmorficzny-zróżnicowana niepełnosprawność intelektualna","synonyms":["NIEAKTUALNE: Mnogie wady wrodzone uwarunkowane genetycznie - zmienna niepełnosprawność intelektualna z dysmorfią lub bez"]},"cs":{"name":"NEAKTUÁLNÍ: Syndromy zahrnující geneticky podmíněné mnohočetné vrozené vady/dysmorfické syndromy a proměnlivou mentální retardaci","synonyms":["NEAKTUÁLNÍ: Geneticky podmíněné MCA/proměnlivá MR","NEAKTUÁLNÍ: Syndrom zahrnující geneticky podmíněné mnohočetné vrozené vady a proměnlivou mentální retardaci, s nebo bez dysmorfismu"]},"uk":{"name":"ЗАСТАРІЛО: Генетично обумовлені множинні вроджені аномалії/дисморфічний синдром/синдром варіабельної розумової відсталості","synonyms":["ЗАСТАРІЛО: Генетичний MCA/варіабельний МР","ЗАСТАРІЛО: Генетичні множинні вроджені аномалії - варіабельна розумова відсталість із синдромом дисморфізму або без нього"]},"zh":{"name":"遗传性多发性先天性异常/畸形综合征-多样性智力障碍综合征","synonyms":["遗传性MCA/多样性 MR"]},"tr":{"name":"Genetik çoklu doğumsal anomaliler/dismorfik sendrom-değişken zihinsel yetersizlik sendromu","synonyms":["Dismorfizm sendromu olan veya olmayan genetik çoklu doğumsal anomaliler-değişken zihinsel yetersizlik","Genetik MCA / değişken MR"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":611327,"name":"Genetic multiple congenital anomalies/dysmorphic syndrome-intellectual disability"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}