{"orpha":474347,"name":"Rare congenital anomaly of ventricular septum","type":"Clinical group","group":"Group of disorders","status":"active","flags":[],"synonyms":["Congenital anomaly of interventricular communication","Congenital ventricular septal anomaly"],"definition":null,"note":"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.","url":"https://raremap.alftech.space/d/ORPHA-474347/","orphanet_url":"https://www.orpha.net/en/disease/detail/474347","names":{"fr":{"name":"Anomalie congénitale du septum interventriculaire rare"},"de":{"name":"Seltene kongenitale Anomalie des Ventrikelseptums","synonyms":["Kongenitale Anomalie der interventrikulären Kommunikation","Ventrikelseptum-Anomalie, kongenitale"]},"es":{"name":"Anomalía congénita rara del septo ventricular","synonyms":["Anomalía congénita de la comunicación interventricular","Anomalía septal ventricular congénita"]},"it":{"name":"Anomalia congenita del setto ventricolare"},"nl":{"name":"Zeldzame congenitale anomalie van ventrikelseptum","synonyms":["Congenitaal ventrikelseptumdefect","Congenitale anomalie van interventriculaire communicatie"]},"pt":{"name":"Anomalia congénita do septo ventricular"},"pl":{"name":"Wrodzona wada przegrody międzykomorowej","synonyms":["Congenital anomaly of interventricular communication","Congenital ventricular septal anomaly"]},"cs":{"name":"Vzácný vrozený defekt komorového septa","synonyms":["Congenital anomaly of interventricular communication","Congenital ventricular septal anomaly"]},"uk":{"name":"Рідкісна вроджена аномалія міжшлуночкової перегородки","synonyms":["Вроджена аномалія міжшлуночкової комунікації","Вроджена аномалія міжшлуночкової перегородки"]},"zh":{"name":"罕见的先天性室间隔发育异常","synonyms":["先天性室间隔异常"]},"tr":{"name":"Nadir doğumsal ventriküler septum anomalisi","synonyms":["Doğumsal ventriküler septal anomali","İnterventriküler iletimin doğumsal anomalisi"]}},"xrefs":[{"source":"MONDO","code":"18771","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680111","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":99096,"name":"OBSOLETE: Multiple ventricular septal defects","status":"inactive"},{"type":"Referred to","orpha":99097,"name":"OBSOLETE: Single ventricular septal defect","status":"inactive"}],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":88991,"name":"Rare congenital heart disease","classifications":[147,148]}],"children":[{"orpha":99092,"name":"Interventricular septum aneurysm","type":"Morphological anomaly"},{"orpha":99094,"name":"Laubry-Pezzi syndrome","type":"Morphological anomaly"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}