Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Mar 2022. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4970045015 | Catecholaminergic polymorphic ventricular tachycardia due to calsequestrin mutation (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4970046019 | Catecholaminergic polymorphic ventricular tachycardia due to calsequestrin mutation | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Catecholaminergic polymorphic ventricular tachycardia due to calsequestrin mutation (disorder) | Is a | Catecholaminergic polymorphic ventricular tachycardia (disorder) | true | Inferred relationship | Some | ||
| Catecholaminergic polymorphic ventricular tachycardia due to calsequestrin mutation (disorder) | Finding site | Structure of ventricular conducting pathway (body structure) | true | Inferred relationship | Some | 2 | |
| Catecholaminergic polymorphic ventricular tachycardia due to calsequestrin mutation (disorder) | Interprets | Heart rate | true | Inferred relationship | Some | 1 | |
| Catecholaminergic polymorphic ventricular tachycardia due to calsequestrin mutation (disorder) | Has interpretation | Increased | true | Inferred relationship | Some | 1 | |
| Catecholaminergic polymorphic ventricular tachycardia due to calsequestrin mutation (disorder) | Is a | Cardiac complication | true | Inferred relationship | Some | ||
| Catecholaminergic polymorphic ventricular tachycardia due to calsequestrin mutation (disorder) | Due to | Chromosomal disorder (disorder) | true | Inferred relationship | Some | 3 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR