Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3663008016 | Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3663009012 | Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3663010019 | Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation | Finding site | Myocardium structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation | Finding site | Cardiac conducting system structure | true | Inferred relationship | Existential restriction modifier | 2 | |
| Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation | Is a | Familial cardiomyopathy | true | Inferred relationship | Existential restriction modifier | ||
| Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation | Is a | Cardiovascular system hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation | Is a | Congestive cardiomyopathy | true | Inferred relationship | Existential restriction modifier | ||
| Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation | Associated morphology | Dilatation | true | Inferred relationship | Existential restriction modifier | 1 | |
| Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation | Is a | Conduction disorder of the heart | true | Inferred relationship | Existential restriction modifier | ||
| Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR