Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3303977011 | Familial isolated arrhythmogenic right ventricular dysplasia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3303978018 | Familial isolated arrhythmogenic right ventricular dysplasia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3303979014 | Familial isolated ARVD (arrhythmogenic right ventricular dysplasia) | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3303980012 | Familial isolated arrhythmogenic right ventricular cardiomyopathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5401146018 | Familial isolated arrhythmogenic right ventricular dysplasia (ARVC) is the familial autosomal dominant form of ARVC, a heart muscle disease characterized by life-threatening ventricular arrhythmias with left bundle branch block configuration that may manifest with palpitations, ventricular tachycardia, syncope and sudden fatal attacks, and that is due to dystrophy and fibro-fatty replacement of the right ventricular myocardium that may lead to right ventricular aneurysms. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5401147010 | Familial isolated arrhythmogenic right ventricular dysplasia (ARVC) is the familial autosomal dominant form of ARVC, a heart muscle disease characterised by life-threatening ventricular arrhythmias with left bundle branch block configuration that may manifest with palpitations, ventricular tachycardia, syncope and sudden fatal attacks, and that is due to dystrophy and fibro-fatty replacement of the right ventricular myocardium that may lead to right ventricular aneurysms. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial isolated arrhythmogenic right ventricular dysplasia (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Familial isolated arrhythmogenic right ventricular dysplasia (disorder) | Is a | Arrhythmogenic right ventricular dysplasia (disorder) | true | Inferred relationship | Some | ||
| Familial isolated arrhythmogenic right ventricular dysplasia (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 1 | |
| Familial isolated arrhythmogenic right ventricular dysplasia (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 1 | |
| Familial isolated arrhythmogenic right ventricular dysplasia (disorder) | Finding site | Right cardiac ventricular structure (body structure) | false | Inferred relationship | Some | 1 | |
| Familial isolated arrhythmogenic right ventricular dysplasia (disorder) | Pathological process (attribute) | Pathological developmental process | false | Inferred relationship | Some | 1 | |
| Familial isolated arrhythmogenic right ventricular dysplasia (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| Familial isolated arrhythmogenic right ventricular dysplasia (disorder) | Finding site | Structure of myocardium of right ventricle | true | Inferred relationship | Some | 1 | |
| Familial isolated arrhythmogenic right ventricular dysplasia (disorder) | Finding site | Cardiac conducting system structure | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
FHIR