Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Keratosis palmoplantaris and arrhythmogenic cardiomyopathy syndrome (disorder) | Is a | True | Arrhythmogenic right ventricular dysplasia (disorder) | Inferred relationship | Existential restriction modifier (core metadata concept) | |
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. | Is a | True | Arrhythmogenic right ventricular dysplasia (disorder) | Inferred relationship | Existential restriction modifier (core metadata concept) |
This concept is not in any reference sets