Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3439441017 | Atrial septal defect, atrioventricular conduction defect syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3439442012 | Atrial septal defect, atrioventricular conduction defect syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3439443019 | An extremely rare genetic congenital heart disease with the presence of atrial septal defect, mostly of the ostium secundum type, associated with conduction anomalies like atrioventricular block, atrial fibrillation or right bundle branch block. There is evidence this disease is caused by heterozygous mutation in the NKX2-5 gene on chromosome 5q35. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 892421000172113 | syndrome de communication interauriculaire-trouble de la conduction atrioventriculaire | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| 1937861000172118 | syndrome de communication interatriale-trouble de la conduction atrioventriculaire | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| 1937871000172110 | syndrome de communication interauriculaire-trouble de la conduction auriculoventriculaire | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| 945541000172111 | atriumseptumdefect, atrioventriculaire geleidingsdefecten-syndroom | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| 1937881000172113 | syndroom van atriumseptumdefect en atrioventriculair geleidingsdefect | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Atrial septal defect, atrioventricular conduction defect syndrome (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Atrial septal defect, atrioventricular conduction defect syndrome (disorder) | Is a | Cardiovascular system hereditary disorder | true | Inferred relationship | Some | ||
| Atrial septal defect, atrioventricular conduction defect syndrome (disorder) | Is a | Congenital atrial septal defect (disorder) | true | Inferred relationship | Some | ||
| Atrial septal defect, atrioventricular conduction defect syndrome (disorder) | Is a | Cardiac arrhythmia associated with genetic disorder (disorder) | true | Inferred relationship | Some | ||
| Atrial septal defect, atrioventricular conduction defect syndrome (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 2 | |
| Atrial septal defect, atrioventricular conduction defect syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
| Atrial septal defect, atrioventricular conduction defect syndrome (disorder) | Finding site | Interatrial septum structure | false | Inferred relationship | Some | 2 | |
| Atrial septal defect, atrioventricular conduction defect syndrome (disorder) | Associated morphology | defect | false | Inferred relationship | Some | 3 | |
| Atrial septal defect, atrioventricular conduction defect syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
| Atrial septal defect, atrioventricular conduction defect syndrome (disorder) | Finding site | Interatrial septum structure | false | Inferred relationship | Some | 3 | |
| Atrial septal defect, atrioventricular conduction defect syndrome (disorder) | Associated morphology | defect | false | Inferred relationship | Some | 1 | |
| Atrial septal defect, atrioventricular conduction defect syndrome (disorder) | Finding site | Interatrial septum structure | true | Inferred relationship | Some | 1 | |
| Atrial septal defect, atrioventricular conduction defect syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Atrial septal defect, atrioventricular conduction defect syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Atrial septal defect, atrioventricular conduction defect syndrome (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
| Atrial septal defect, atrioventricular conduction defect syndrome (disorder) | Associated morphology | Abnormal communication | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR