Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3321517012 | Cardiac anomaly and heterotaxy syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3321518019 | Cardiac anomaly and heterotaxy syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3321519010 | This syndrome has characteristics of non-compaction of the ventricular myocardium, bradycardia, pulmonary valve stenosis and secundum atrial septal defect. Laterality sequence anomalies are also present. So far, the syndrome has been described in nine members from three generations of the same family. Transmission is autosomal dominant and linkage to chromosome 6p24.3-21.2 was reported. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Cardiac anomaly and heterotaxy syndrome (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Cardiac anomaly and heterotaxy syndrome (disorder) | Is a | Congenital heart disease | true | Inferred relationship | Some | ||
Cardiac anomaly and heterotaxy syndrome (disorder) | Is a | Situs ambiguus | true | Inferred relationship | Some | ||
Cardiac anomaly and heterotaxy syndrome (disorder) | Is a | Cardiovascular system hereditary disorder | true | Inferred relationship | Some | ||
Cardiac anomaly and heterotaxy syndrome (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 1 | |
Cardiac anomaly and heterotaxy syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Cardiac anomaly and heterotaxy syndrome (disorder) | Finding site | Heart structure | true | Inferred relationship | Some | 1 | |
Cardiac anomaly and heterotaxy syndrome (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
Cardiac anomaly and heterotaxy syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Cardiac anomaly and heterotaxy syndrome (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Cardiac anomaly and heterotaxy syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Cardiac anomaly and heterotaxy syndrome (disorder) | Finding site | Structure of viscus | true | Inferred relationship | Some | 2 | |
Cardiac anomaly and heterotaxy syndrome (disorder) | Associated morphology | Malposition (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
Cardiac anomaly and heterotaxy syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets