{"orpha":79446,"name":"Multiple pterygium syndrome, Aslan type","type":"Etiological subtype","group":"Subtype of 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 Bartsocas-Papas syndrome","url":"https://raremap.alftech.space/d/ORPHA-79446/","orphanet_url":"https://www.orpha.net/en/disease/detail/79446","names":{"fr":{"name":"Syndrome des ptérygium multiples type Aslan"},"de":{"name":"Multiples Pterygium-Syndrom Typ Aslan"},"es":{"name":"Síndrome de pterigium múltiple tipo Aslan"},"it":{"name":"Sindrome dei pterigi multipli, tipo Aslan"},"nl":{"name":"Meervoudig pterygium-syndroom, Aslan-type"},"pt":{"name":"Síndrome de pterígio múltiplo, tipo Aslan"},"pl":{"name":"Zespół mnogich płetwistości typu Aslana"},"cs":{"name":"Syndrom mnohočetných pterygií, Aslanův typ"},"uk":{"name":"Синдром множинних птеригіумів, тип Аслана"},"zh":{"name":"致死性腿部翼状带综合征"},"tr":{"name":"Çoklu piterjiyum sendromu, Aslan tipi"}},"xrefs":[],"associations":[{"type":"Moved to","orpha":1234,"name":"Bartsocas-Papas syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}