{"orpha":137911,"name":"Autism-facial port-wine stain syndrome","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":[],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Sturge-Weber syndrome","url":"https://raremap.alftech.space/d/ORPHA-137911/","orphanet_url":"https://www.orpha.net/en/disease/detail/137911","names":{"fr":{"name":"Syndrome d'autisme-angiome facial"},"de":{"name":"Autismus-fazialer Portwein-Nävus-Syndrom"},"es":{"name":"Síndrome de autismo-mancha facial en vino de Oporto"},"it":{"name":"Autismo - nevo vinoso facciale"},"nl":{"name":"Autisme - faciale wijnvlek-syndroom","synonyms":["Autisme - faciale naevus flammeus-syndroom"]},"pt":{"name":"Síndrome de autismo-mancha facial vinho do porto"},"pl":{"name":"Autyzm - znamię naczyniowe twarzy typu \"port-wine stain"},"cs":{"name":"Syndrom zahrnující autismus a faciální naevus flammeus"},"uk":{"name":"Синдром аутизму-портвейнової плями обличчя"},"zh":{"name":"孤独症-面部葡萄酒色斑综合征","definition":"该综合征的特征是面部出现单侧血管瘤和以语言迟缓和不典型的社会互动为特点的自闭症发育障碍。"},"tr":{"name":"Otizm-yüz porto şarabı lekesi sendromu"}},"xrefs":[{"source":"GARD","code":"10303","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":3205,"name":"Sturge-Weber syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}