Status: current, Defined. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 59588016 | Familial cardiomyopathy | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 59589012 | Primary familial cardiomyopathy | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 767399015 | Familial cardiomyopathy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial cardiomyopathy | Is a | Familial disease | true | Inferred relationship | Some | ||
| Familial cardiomyopathy | Is a | Primary cardiomyopathy | false | Inferred relationship | Some | ||
| Familial cardiomyopathy | Is a | Cardiovascular system hereditary disorder | false | Inferred relationship | Some | ||
| Familial cardiomyopathy | Is a | Cardiomyopathy | true | Inferred relationship | Some | ||
| Familial cardiomyopathy | Finding site | Myocardium structure | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Danish type familial amyloid cardiomyopathy | Is a | True | Familial cardiomyopathy | Inferred relationship | Some | |
| Familial restrictive cardiomyopathy | Is a | True | Familial cardiomyopathy | Inferred relationship | Some | |
| Restrictive cardiomyopathy secondary to familial storage disease | Is a | False | Familial cardiomyopathy | Inferred relationship | Some | |
| Primary familial dilated cardiomyopathy | Is a | False | Familial cardiomyopathy | Inferred relationship | Some | |
| Dilated cardiomyopathy due to familial storage disease | Is a | False | Familial cardiomyopathy | Inferred relationship | Some | |
| Primary familial hypertrophic cardiomyopathy | Is a | True | Familial cardiomyopathy | Inferred relationship | Some | |
| Primary familial dilated cardiomyopathy | Is a | True | Familial cardiomyopathy | Inferred relationship | Some | |
| Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation | Is a | True | Familial cardiomyopathy | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Cardiovascular finding reference set
Problem/Diagnosis reference set
FHIR