{"orpha":98731,"name":"OBSOLETE: Congenital arteriovenous fistula","type":"Category","group":"Group of disorders","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Rare vascular anomaly","url":"https://raremap.alftech.space/d/ORPHA-98731/","orphanet_url":"https://www.orpha.net/en/disease/detail/98731","names":{"fr":{"name":"OBSOLETE : Fistule artérioveineuse congénitale"},"de":{"name":"OBSOLET: Kongenitale arteriovenöse Fistel"},"es":{"name":"OBSOLETO: Fístula arteriovenosa congénita"},"it":{"name":"OBSOLETO: Fistola arterovenosa congenita"},"nl":{"name":"OBSOLEET: Congenitale arterioveneuze fistel"},"pt":{"name":"OBSOLETO: Fístula arteriovenosa"},"pl":{"name":"NIEAKTUALNE: Wrodzona przetoka tętniczo-żylna"},"cs":{"name":"NEAKTUÁLNÍ: Vrozené arteriovenózní píštěle"},"uk":{"name":"Вроджена артеріовенозна фістула","definition":"A rare simple vascular malformation characterized by a congenital abnormal connection between an artery and a vein, appearing as varicose veins with port wine discoloration, leading to a bypass of the capillary bed. Signs and symptoms include palpable continuous thrill in the dilated vessels, continuous machinery murmur with systolic accentuation, collapsing arterial pulse, Nicoladoni Branham sign, as well as local gigantism and hot ulcers due to hypoxia, among others."},"zh":{"name":"先天性动静脉瘘","definition":"一种罕见的单纯性血管畸形，其特征是动脉和静脉之间的先天异常连接，表现为静脉曲张，伴有鲜红酒变色，导致毛细血管床旁路开放。体征和症状包括扩张的血管中可触摸到的持续性震颤，伴有收缩期加重的持续性机械杂音，动脉脉搏收缩，Nicoladoni Branham征，以及由于缺氧而导致的局部肿大和热溃疡等。"},"tr":{"name":"Doğumsal arteriyovenöz fistül"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":68419,"name":"Rare vascular anomaly"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}