{"orpha":99097,"name":"OBSOLETE: Single ventricular septal defect","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 congenital anomaly of ventricular septum","url":"https://raremap.alftech.space/d/ORPHA-99097/","orphanet_url":"https://www.orpha.net/en/disease/detail/99097","names":{"fr":{"name":"OBSOLETE : Communication interventriculaire unique"},"de":{"name":"OBSOLET: Ventrikelseptumdefekt, einfacher"},"es":{"name":"OBSOLETO: CIV simple"},"it":{"name":"OBSOLETO: DIV isolato"},"nl":{"name":"OBSOLEET: Enkelvoudig ventikelseptumdefect"},"pt":{"name":"OBSOLETO: Defeito único do septo ventricular"},"pl":{"name":"NIEAKTUALNE: Pojedynczy ubytek przegrody miedzykomorowej"},"cs":{"name":"NEAKTUÁLNÍ: Jednoduchý defekt komorového septa"},"uk":{"name":"ЗАСТАРІЛО: Дефект міжшлуночкової перетинки в серці з єдиним шлуночком"},"zh":{"name":"弃用：单发室间隔缺损"},"tr":{"name":"Eski adı: Tek ventriküler septal defekt"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":474347,"name":"Rare congenital anomaly of ventricular septum"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}