{"orpha":2039,"name":"OBSOLETE: Congenital systemic arteriovenous fistula","type":"Morphological anomaly","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Rare vascular anomaly","url":"https://raremap.alftech.space/d/ORPHA-2039/","orphanet_url":"https://www.orpha.net/en/disease/detail/2039","names":{"fr":{"name":"OBSOLETE : Fistule artérioveineuse systémique congénitale"},"de":{"name":"OBSOLET: Kongenitale systemische arteriovenöse Fistel"},"es":{"name":"OBSOLETO: Fístula arteriovenosa sistémica congénita"},"it":{"name":"OBSOLETO: Fistola arterovenosa sistemica congenita"},"nl":{"name":"OBSOLEET: Congenitale systemische arterioveneuze fistel"},"pt":{"name":"OBSOLETO: Fístula arterio-venosa sistémica"},"pl":{"name":"NIEAKTUALNE: Wrodzona systemowa przetoka tętniczo-żylna"},"cs":{"name":"NEAKTUÁLNÍ: Vrozená systémová arteriovenózní píštěl"},"uk":{"name":"Вроджена системна артеріовенозна фістула","definition":"Congenital systemic arteriovenous fistula is a rare, potentially life-threatening, vascular malformation characterized by a direct communication between an artery and a vein, without the interposition of the capillary bed, ocurring in the systemic circulation (mainly the cranium, liver, lungs, extremities, and vessels in or near the thoracic wall). Manifestations are variable depending on size and extent of the fistula, the involved blood vessels and the precise location of the collaterals and may include systolic or continuous murmur over the affected organ, tachycardia, increased stroke volume, cardiomegaly and increased pulmonary vascular markings."},"zh":{"name":"先天性体循环动静脉瘘"},"tr":{"name":"Doğumsal sistemik 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}