Status: current, Primitive. Date: 28-Feb 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4952427019 | Catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
4952428012 | Catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation | Is a | Cardiac complication | true | Inferred relationship | Some | ||
Catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation | Is a | Catecholaminergic polymorphic ventricular tachycardia | true | Inferred relationship | Some | ||
Catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation | Due to | Chromosomal disorder | true | Inferred relationship | Some | 3 | |
Catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation | Finding site | Ventricular conducting pathway | true | Inferred relationship | Some | 2 | |
Catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation | Interprets | Heart rate | true | Inferred relationship | Some | 1 | |
Catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation | Has interpretation | Increased | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Cardiovascular finding reference set
Problem/Diagnosis reference set