Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2011. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2897983016 | Congenital prolapse of aortic valve (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2899714015 | Congenital aortic valvar prolapse | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2899715019 | Congenital prolapse of aortic valve | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital prolapse of aortic valve (disorder) | Is a | Abnormal position of cardiac valve | false | Inferred relationship | Some | ||
| Congenital prolapse of aortic valve (disorder) | Is a | Cardiac valve prolapse (disorder) | true | Inferred relationship | Some | ||
| Congenital prolapse of aortic valve (disorder) | Is a | Abnormality of aortic valve (disorder) | false | Inferred relationship | Some | ||
| Congenital prolapse of aortic valve (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Congenital prolapse of aortic valve (disorder) | Finding site | Aortic valve structure | true | Inferred relationship | Some | 1 | |
| Congenital prolapse of aortic valve (disorder) | Associated morphology | kongenit prolaps | false | Inferred relationship | Some | 1 | |
| Congenital prolapse of aortic valve (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
| Congenital prolapse of aortic valve (disorder) | Associated morphology | kongenit prolaps | false | Inferred relationship | Some | 2 | |
| Congenital prolapse of aortic valve (disorder) | Finding site | Aortic valve structure | false | Inferred relationship | Some | 2 | |
| Congenital prolapse of aortic valve (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Congenital prolapse of aortic valve (disorder) | Is a | Congenital anomaly of cardiac chamber (disorder) | false | Inferred relationship | Some | ||
| Congenital prolapse of aortic valve (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Congenital prolapse of aortic valve (disorder) | Is a | Congenital anomaly of aortic valve | true | Inferred relationship | Some | ||
| Congenital prolapse of aortic valve (disorder) | Associated morphology | Prolapse | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Laubry-Pezzi syndrome is a rare, non-syndromic, congenital heart malformation characterized by the prolapse of an aortic valve cusp into a subjacent ventricular septal defect due to Venturi effect, resulting in aortic regurgitation. Patients typically present with symptoms of progressive aortic valve insufficiency, such as shortness of breath, heart palpitations, chest pain and exercise intolerance. | Is a | True | Congenital prolapse of aortic valve (disorder) | Inferred relationship | Some |
This concept is not in any reference sets
FHIR