{"orpha":199627,"name":"Atypical autism","type":"Disease","group":"Disorder","status":"active","flags":[],"synonyms":[],"definition":"A rare, pervasive developmental disorder that does not fit the diagnosis for the other specific autistic spectrum disorders (autism, Asperger syndrome, Rett syndrome or childhood disintegrative disorder) and is characterized by usually milder developmental and social delay and less stereotypical autistic behavior.","note":null,"url":"https://raremap.alftech.space/d/ORPHA-199627/","orphanet_url":"https://www.orpha.net/en/disease/detail/199627","names":{"fr":{"name":"Autisme atypique","definition":"L'autisme atypique est un trouble envahissant du développement qui ne correspond pas au diagnostic des autres troubles autistiques spécifiques (l'autisme, le syndrome d'Asperger, le syndrome de Rett ou le syndrome désintégratif de l'enfance;). Il est caractérisé par un retard du développement généralement plus léger et une prévalence inférieure de comportements stéréotypés de type autistique."},"de":{"name":"Autismus, atypischer","definition":"Der Atypische Autismus ist eine universelle Entwicklungsstörung, die nicht in das diagnostische Schema der anderen Autismusspektrum-Störungen (Autismus, Asperger-Syndrom, Rett-Syndrom oder Disintegrative Störung des Kindesalters) passt. Die Krankheit ist gekennzeichnet durch meist mildere Ausprägungen der Entwicklungsverzögerung und der Störung des Sozialverhaltens und durch weniger ausgeprägte stereotype autistoide Verhaltensweisen."},"es":{"name":"Autismo atípico","definition":"Es un trastorno generalizado del desarrollo que no encaja en el diagnóstico de los otros trastornos específicos del espectro autista (autismo, síndrome de Asperger, síndrome de Rett, o trastorno desintegrativo de la infancia; consulte estos términos) y se caracteriza por un retraso del desarrollo y social normalmente más leve, y un comportamiento autista menos estereotipado."},"it":{"name":"Autismo atipico","definition":"L'autismo atipico è un disturbo pervasivo dello sviluppo che non rientra negli altri disturbi specifici dello spettro autistico (autismo, sindrome di Asperger, sindrome di Rett o disturbo disintegrativo dell'infanzia; si vedano questi termini); è caratterizzato di solito da un ritardo nell'integrazione sociale e nello sviluppo, di solito lievi, e da un comportamento autistico meno stereotipato."},"nl":{"name":"Atypisch autisme","definition":"Een zeldzame, pervasieve ontwikkelingsstoornis die niet voldoet aan de diagnose van de andere specifieke autismespectrumstoornissen (autisme, syndroom van Asperger, syndroom van Rett of desintegratieve stoornis in de kindertijd) en die gekarakteriseerd wordt door doorgaans mildere ontwikkelings- en sociale achterstand en minder stereotiep autistisch gedrag."},"pt":{"name":"Autismo atípico"},"pl":{"name":"Autyzm atypowy"},"cs":{"name":"Atypický autismus"},"uk":{"name":"Атиповий аутизм","definition":"A rare, pervasive developmental disorder that does not fit the diagnosis for the other specific autistic spectrum disorders (autism, Asperger syndrome, Rett syndrome or childhood disintegrative disorder) and is characterized by usually milder developmental and social delay and less stereotypical autistic behavior."},"zh":{"name":"非典型孤独症谱系障碍","definition":"非典型自闭症是一种罕见的广泛性发育障碍，不能归类于其它特异性的自闭症光谱疾病（自闭症、Asperger综合征、雷特综合征或儿童崩解症），其特征为发育障碍和社交障碍症状较轻，典型自闭症行为较少。"},"tr":{"name":"Atipik otizm"}},"xrefs":[{"source":"ICD-10","code":"F84.1","qualifier":"E","icd_relation":"specific","validated":true},{"source":"ICD-11","code":"6A02.Y","qualifier":"NTBT","icd_relation":"index","validated":true,"icd11_uri":"2136163538"},{"source":"MONDO","code":"0016052","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0338986","qualifier":"E","icd_relation":null,"validated":true},{"source":"MedDRA","code":"10003747","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":168778,"name":"Rare pervasive developmental disorder","classifications":[156,181]}],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}