Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3307115013 | Congenital infection caused by Epstein-Barr virus (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| 3307116014 | Congenital infection caused by Epstein-Barr virus | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3307117017 | Congenital Epstein-Barr virus infection | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3307118010 | Congenital infection caused by Human herpesvirus 4 | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital infection caused by Epstein-Barr virus | Is a | Epstein-Barr virus disease | true | Inferred relationship | Existential restriction modifier | ||
| Congenital infection caused by Epstein-Barr virus | Is a | Congenital infection caused by Herpes virus | true | Inferred relationship | Existential restriction modifier | ||
| Congenital infection caused by Epstein-Barr virus | Causative agent | Human herpesvirus 4 | true | Inferred relationship | Existential restriction modifier | 1 | |
| Congenital infection caused by Epstein-Barr virus | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Congenital infection caused by Epstein-Barr virus | Pathological process | Infectious process | true | Inferred relationship | Existential restriction modifier | 1 | |
| Congenital infection caused by Epstein-Barr virus | Is a | Disease caused by Gammaherpesvirinae | false | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR