{"orpha":53719,"name":"OBSOLETE: Cerebrofacial arteriovenous metameric syndrome type 2","type":"Clinical subtype","group":"Subtype of disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: Bonnet-Dechaume-Blanc syndrome","OBSOLETE: CAMS2","OBSOLETE: Wyburn-Mason syndrome"],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Cerebrofacial arteriovenous metameric syndrome","url":"https://raremap.alftech.space/d/ORPHA-53719/","orphanet_url":"https://www.orpha.net/en/disease/detail/53719","names":{"fr":{"name":"OBSOLETE : Syndrome métamérique artérioveineux cérébro-facial type 2","synonyms":["OBSOLETE : CAMS2","OBSOLETE : Syndrome de Bonnet-Dechaume-Blanc","OBSOLETE : Syndrome de Wyburn-Mason"]},"de":{"name":"OBSOLET: Zerebrofaziales arteriovenöses metameres Syndrom Typ 2","synonyms":["OBSOLET: CAMS2","OBSOLET: Wyburn-Mason-Syndrom","OBSOLET: Bonnet-Dechaume-Blanc-Syndrom"]},"es":{"name":"OBSOLETO: Síndrome arteriovenoso cerebrofacial metamérico tipo 2","synonyms":["OBSOLETO: Síndrome de Wyburn-Mason","OBSOLETO: Síndrome de Bonnet-Dechaume-Blanc","OBSOLETO: CAMS2"]},"it":{"name":"OBSOLETO: Sindrome di Wyburn-Mason","synonyms":["OBSOLETO: CAMS2","OBSOLETO: Sindrome di Bonnet-Dechaume-Blanc","OBSOLETO: Sindrome metamerica arterovenosa cerebrofacciale, tipo 2"]},"nl":{"name":"OBSOLEET: Cerebrofaciaal arterioveneus metamerisch syndroom type 2","synonyms":["NIET ZELDZAME ZIEKTE IN EUROPA: CAMS2","NIET ZELDZAME ZIEKTE IN EUROPA: Syndroom van Wyburn-Mason","NIET ZELDZAME ZIEKTE IN EUROPA: Syndroom van Bonnet-Dechaume-Blanc"]},"pt":{"name":"OBSOLETO: Síndrome metamérico arteriovenoso cerebrofacial tipo 2","synonyms":["OBSOLETO: Síndrome Wyburn-Mason","OBSOLETO: Síndrome Bonnet-Dechaume-Blanc","OBSOLETO: CAMS2"]},"pl":{"name":"NIEAKTUALNE: Zespół Wyburna i Masona","synonyms":["NIEAKTUALNE: CAMS2","NIEAKTUALNE: Zespół Bonneta, Dechaume'a i Blanca","NIEAKTUALNE: Zespół mózgowo-twarzowy tętniczo-żylny metameryczny typu 2","NIEAKTUALNE: Zespół metameryczny tętniczo-żylny mózgowo-twarzowy typu 2"]},"cs":{"name":"NEAKTUÁLNÍ: Wyburn-Masonův syndrom","synonyms":["NEAKTUÁLNÍ: CAMS2","NEAKTUÁLNÍ: Cerebrofaciální arteriovenózní metamerický syndrom, typ 2","NEAKTUÁLNÍ: Bonnetův-Dechaumeův-Blancův syndrom","NEAKTUÁLNÍ: Bonnet-Dechaume-Blancův syndrom"]},"uk":{"name":"Синдром Вайберна-Мейсона","synonyms":["Синдром Бонне-Дешома-Блана","CAMS2","Цереброфасціальний артеріовенозний метамерний синдром, тип 2"],"definition":"Wyburn-Mason syndrome or Bonnet-Dechaume-Blanc syndrome is characterized by the association of arteriovenous malformations of the maxilla, retina, optic nerve, thalamus, hypothalamus and cerebral cortex."},"zh":{"name":"脑-视网膜动静脉瘤综合征","synonyms":["脑面部动静脉异构综合征2型"]},"tr":{"name":"Wyburn-Mason sendromu","synonyms":["CAMS2","Bonnet-Dechaume-Blanc sendromu","Serebrofasiyal arteriyovenöz metamerik sendrom tip 2"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":141189,"name":"Cerebrofacial arteriovenous metameric syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}