Status: current, Defined. Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3311244016 | Congenital dysplasia of cardiac valve (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3311245015 | Congenital dysplasia of cardiac valve | en | Synonym | Active | Case insensitive | SNOMED CT core |
3311246019 | Congenital valvular dysplasia | en | Synonym | Active | Case insensitive | SNOMED CT core |
3311247011 | A rare entity usually diagnosed by echocardiography. It may be limited to one of the four valves but can also involve the two atrioventricular valves and the two semilunar valves. May be the hallmark of genetic anomalies. Chromosomal anomalies should be searched when polyvalvular dysplasia is found in a fetus, namely trisomy 18 and trisomy 13. Triscuspid valve dysplasia can be the only cardiac finding in trisomy 21 and a karyotype analysis should be performed in all fetuses exhibiting this anomaly. In the absence of chromosomal anomalies, polyvalvular dysplasia can be observed in Noonan syndrome. Thickening of the different cardiac valves can be observed in various storage diseases such as mucopolysaccharidoses. In these later conditions, it develops after the neonatal period and is frequently associated with extracardiac symptoms suggestive of the diagnosis. | en | Definition | Inactive | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital dysplasia of cardiac valve | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Congenital dysplasia of cardiac valve | Associated morphology | Dysplasia | true | Inferred relationship | Some | 1 | |
Congenital dysplasia of cardiac valve | Is a | Congenital anomaly of heart valve | true | Inferred relationship | Some | ||
Congenital dysplasia of cardiac valve | Associated morphology | Congenital dysplasia | false | Inferred relationship | Some | 1 | |
Congenital dysplasia of cardiac valve | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Congenital dysplasia of cardiac valve | Finding site | Cardiac valve structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Congenital dysplasia of aortic valve | Is a | True | Congenital dysplasia of cardiac valve | Inferred relationship | Some | |
Congenital dysplasia of truncal valve | Is a | True | Congenital dysplasia of cardiac valve | Inferred relationship | Some | |
Congenital dysplasia of tricuspid valve | Is a | True | Congenital dysplasia of cardiac valve | Inferred relationship | Some | |
Mitral valve dysplasia | Is a | True | Congenital dysplasia of cardiac valve | Inferred relationship | Some | |
Truncal valve dysplasia | Is a | False | Congenital dysplasia of cardiac valve | Inferred relationship | Some | |
Pulmonary valve dysplasia | Is a | True | Congenital dysplasia of cardiac valve | Inferred relationship | Some | |
Polyvalvular heart disease syndrome | Is a | True | Congenital dysplasia of cardiac valve | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Cardiovascular finding reference set
Problem/Diagnosis reference set