{"orpha":271853,"name":"Genetic cardiac anomaly","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"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-271853/","orphanet_url":"https://www.orpha.net/en/disease/detail/271853","names":{"fr":{"name":"Anomalie cardiaque d'origine génétique"},"de":{"name":"Herzanomalie, genetisch bedingte"},"es":{"name":"Anomalía cardíaca de origen genético"},"it":{"name":"Anomalia cardiaca genetica"},"nl":{"name":"Genetische hartanomalie"},"pt":{"name":"Anomalia cardíaca, genética"},"pl":{"name":"Wada serca uwarunkowana genetycznie"},"cs":{"name":"Geneticky podmíněné anomálie srdce"},"uk":{"name":"Генетично обумовлена серцева аномалія"},"zh":{"name":"遗传性心脏异常"},"tr":{"name":"Genetik kalp anomalisi"}},"xrefs":[{"source":"MONDO","code":"17131","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680759","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":183530,"name":"Rare genetic developmental defect during embryogenesis","classifications":[156]}],"children":[{"orpha":98722,"name":"Atrioventricular septal defect","type":"Clinical group"},{"orpha":860,"name":"Congenitally uncorrected transposition of the great arteries","type":"Morphological anomaly"},{"orpha":369891,"name":"Developmental delay-facial dysmorphism syndrome due to MED13L deficiency","type":"Malformation syndrome"},{"orpha":3426,"name":"Double outlet right ventricle","type":"Morphological anomaly"},{"orpha":402075,"name":"Familial bicuspid aortic valve","type":"Morphological anomaly"},{"orpha":741,"name":"Familial mitral valve prolapse","type":"Morphological anomaly"},{"orpha":466729,"name":"Familial patent arterial duct","type":"Morphological anomaly"},{"orpha":1478,"name":"Interatrial communication","type":"Morphological anomaly"},{"orpha":566862,"name":"Left isomerism","type":"Clinical subtype"},{"orpha":97548,"name":"Right isomerism","type":"Clinical subtype"},{"orpha":101063,"name":"Situs inversus totalis","type":"Morphological anomaly"},{"orpha":3193,"name":"Supravalvular aortic stenosis","type":"Morphological anomaly"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}