Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3663008016 | Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3663009012 | Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3663010019 | Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3663011015 | A rare familial dilated cardiomyopathy with characteristics of left ventricular enlargement and/or reduced systolic function preceded or accompanied by significant conduction system disease and/or arrhythmias including bradyarrhythmias, supraventricular or ventricular arrhythmias. Disease onset is usually in early to mid-adulthood. Sudden cardiac death may occur and may be the presenting symptom. In some cases, it is associated with skeletal myopathy and elevated serum creatine kinase. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | localisation d'une constatation (attribut) | structure du myocarde | true | Inferred relationship | Some | 1 | |
| Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | localisation d'une constatation (attribut) | structure du système de conduction cardiaque | true | Inferred relationship | Some | 2 | |
| Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | est un(e) (attribut) | Familial cardiomyopathy | true | Inferred relationship | Some | ||
| Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | est un(e) (attribut) | Cardiovascular system hereditary disorder | true | Inferred relationship | Some | ||
| Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | est un(e) (attribut) | Congestive cardiomyopathy (disorder) | true | Inferred relationship | Some | ||
| Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | morphologie associée (attribut) | dilatation | true | Inferred relationship | Some | 1 | |
| Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | est un(e) (attribut) | trouble de la conduction cardiaque | true | Inferred relationship | Some | ||
| Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | est un(e) (attribut) | Autosomal dominant hereditary disorder | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR