{"orpha":178503,"name":"Dursun syndrome","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":["Pulmonary arterial hypertension-leukopenia-atrial septal defect syndrome"],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency","url":"https://raremap.alftech.space/d/ORPHA-178503/","orphanet_url":"https://www.orpha.net/en/disease/detail/178503","names":{"fr":{"name":"Syndrome de Dursun","synonyms":["Syndrome d'hypertension artérielle pulmonaire-leucopénie-communication interauriculaire"]},"de":{"name":"Dursun-Syndrom","synonyms":["Pulmonale arterielle Hypertonie - Leukopenie - Vorhofseptumdefekt"]},"es":{"name":"Síndrome de Dursun","synonyms":["Hipertensión arterial pulmonar-leucopenia-defecto septal atrial"]},"it":{"name":"Sindrome di Dursun","synonyms":["Ipertensione arteriosa polmonare - leucopenia - difetto del setto atriale","Sindrome di Dursun"]},"nl":{"name":"Syndroom van Dursun","synonyms":["Pulmonale arteriële hypertensie - leukopenie - atriumseptumdefect-syndroom"]},"pt":{"name":"Hipertensão arterial pulmonar - leucopenia - comunicação inter-auricular"},"pl":{"name":"Zespół Dursuna","synonyms":["Nadciśnienie płucne - leukopenia - wada przegrody międzyprzedsionkowej"]},"cs":{"name":"Dursunův syndrom","synonyms":["Syndrom zahrnující plicní arteriální hypertenzi, leukopenii a defekt síňového septa"]},"uk":{"name":"Синдром Дурсуна","synonyms":["Синдром легеневої артеріальної гіпертензії-лейкопенії- дефекту міжпередсердної перегородки"]},"zh":{"name":"Dursun 综合征","synonyms":["肺动脉高压-白细胞减少-房间隔缺损综合征"]},"tr":{"name":"Dursun sendromu","synonyms":["Pulmoner arteriyel hipertansiyon-lökopeni-atriyal septal defekt sendromu"]}},"xrefs":[{"source":"UMLS","code":"C2751630","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":331176,"name":"Severe congenital neutropenia due to G6PC3 deficiency"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}