Status: current, Primitive. 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 | Case insensitive | SNOMED CT core |
3439442012 | Atrial septal defect, atrioventricular conduction defect syndrome | en | Synonym | Active | Case insensitive | 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 | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Atrial septal defect, atrioventricular conduction defect syndrome | Associated morphology | Defect | true | Inferred relationship | Some | 1 | |
Atrial septal defect, atrioventricular conduction defect syndrome | Finding site | Interatrial septum structure | true | Inferred relationship | Some | 1 | |
Atrial septal defect, atrioventricular conduction defect syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Atrial septal defect, atrioventricular conduction defect syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Atrial septal defect, atrioventricular conduction defect syndrome | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Atrial septal defect, atrioventricular conduction defect syndrome | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Atrial septal defect, atrioventricular conduction defect syndrome | Is a | Cardiovascular system hereditary disorder | true | Inferred relationship | Some | ||
Atrial septal defect, atrioventricular conduction defect syndrome | Is a | Congenital atrial septal defect | true | Inferred relationship | Some | ||
Atrial septal defect, atrioventricular conduction defect syndrome | Is a | Cardiac arrhythmia associated with genetic disorder | true | Inferred relationship | Some | ||
Atrial septal defect, atrioventricular conduction defect syndrome | Associated morphology | Developmental abnormality | false | Inferred relationship | Some | 2 | |
Atrial septal defect, atrioventricular conduction defect syndrome | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
Atrial septal defect, atrioventricular conduction defect syndrome | Finding site | Interatrial septum structure | false | Inferred relationship | Some | 2 | |
Atrial septal defect, atrioventricular conduction defect syndrome | Associated morphology | Defect | false | Inferred relationship | Some | 3 | |
Atrial septal defect, atrioventricular conduction defect syndrome | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
Atrial septal defect, atrioventricular conduction defect syndrome | Finding site | Interatrial septum structure | false | Inferred relationship | Some | 3 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Cardiovascular finding reference set
Problem/Diagnosis reference set