{"orpha":168778,"name":"Rare pervasive developmental disorder","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":["Rare ASD","Rare PDD","Rare autism spectrum disorder"],"definition":null,"note":"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.","url":"https://raremap.alftech.space/d/ORPHA-168778/","orphanet_url":"https://www.orpha.net/en/disease/detail/168778","names":{"fr":{"name":"Trouble envahissant du développement rare","synonyms":["TED rare","Trouble rare du spectre de l'autisme"]},"de":{"name":"Seltene tiefgreifende Entwicklungsstörung","synonyms":["Seltene Autismusspektrumstörung"]},"es":{"name":"Trastorno generalizado raro del desarrollo","synonyms":["TEA raro","TGD raro","Trastorno raro del espectro autista"]},"it":{"name":"Disturbo pervasivo dello sviluppo raro","synonyms":["Disturbi rari dello spettro dell'autismo"]},"nl":{"name":"Zeldzame pervasieve ontwikkelingsstoornis","synonyms":["Zeldzame ASS","Zeldzame POS","Zeldzame autismespectrumstoornis"]},"pt":{"name":"Doença global do desenvolvimento"},"pl":{"name":"Rzadkie złożone zaburzenia rozwoju","synonyms":["Rzadkie zaburzenie spektrum autyzmu"]},"cs":{"name":"Vzácné pervazivní vývojové poruchy","synonyms":["Vzácné ASD","Vzácné PDD","Vzácná porucha autistického spektra"]},"uk":{"name":"Рідкісний первазивний розлад розвитку","synonyms":["Рідкісний аутизм","Рідкісний розлад аутистичного спектру","Рідкісні PDD"]},"zh":{"name":"罕见全面发育障碍","synonyms":["罕见自闭症谱系障碍"]},"tr":{"name":"Nadir yaygın gelişimsel bozukluk","synonyms":["Nadir ASD","Nadir PDD","Nadir otizm spektrum bozukluğu"]}},"xrefs":[{"source":"MONDO","code":"15680","qualifier":"E","icd_relation":null,"validated":true},{"source":"MeSH","code":"D002659","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5679581","qualifier":"E","icd_relation":null,"validated":true},{"source":"MedDRA","code":"10061345","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":71859,"name":"Rare genetic neurological disorder","classifications":[156]},{"orpha":98033,"name":"Rare neurologic disease with psychiatric involvement","classifications":[181]}],"children":[{"orpha":3095,"name":"Atypical Rett syndrome","type":"Disease"},{"orpha":199627,"name":"Atypical autism","type":"Disease"},{"orpha":505652,"name":"CDKL5-deficiency disorder","type":"Disease"},{"orpha":168782,"name":"Childhood disintegrative disorder","type":"Disease"},{"orpha":561854,"name":"FOXG1 syndrome","type":"Disease"},{"orpha":600663,"name":"NRXN1-related severe neurodevelopmental disorder-motor stereotypies-chronic constipation-sleep-wake cycle disturbance","type":"Malformation syndrome"},{"orpha":180772,"name":"Rare disease with autism","type":"Category"},{"orpha":778,"name":"Rett syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}