Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 39019015 | Common variable agammaglobulinemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 39020014 | CVAG | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 481559011 | Common variable immunodeficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 481560018 | CVI - Common variable immunodeficiency | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 481561019 | Late onset immunoglobulin deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 481562014 | CVID - Common variable immunodeficiency | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 481563016 | Common variable agammaglobulinaemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 481564010 | Acquired hypogammaglobulinaemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 481565011 | Common variable hypogammaglobulinaemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 481566012 | Acquired hypogammaglobulinemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 481567015 | Common variable hypogammaglobulinemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 752735015 | Common variable agammaglobulinemia (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Common variable agammaglobulinemia | Is a | Congenital agammaglobulinemia | true | Inferred relationship | Existential restriction modifier | ||
| Common variable agammaglobulinemia | Finding site | Structure of immune system | false | Inferred relationship | Existential restriction modifier | ||
| Common variable agammaglobulinemia | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Common variable agammaglobulinemia | Has definitional manifestation | Immune system finding | false | Inferred relationship | Existential restriction modifier | ||
| Common variable agammaglobulinemia | Is a | Hereditary cancer-predisposing syndrome | true | Inferred relationship | Existential restriction modifier | ||
| Common variable agammaglobulinemia | Pathological process | Abnormal immune process | true | Inferred relationship | Existential restriction modifier | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Common variable immunodeficiency with predominant abnormalities of B-cell numbers and functions | Is a | True | Common variable agammaglobulinemia | Inferred relationship | Existential restriction modifier | |
| Common variable immunodeficiency with predominant immunoregulatory T-cell disorders | Is a | True | Common variable agammaglobulinemia | Inferred relationship | Existential restriction modifier | |
| Common variable immunodeficiency with autoantibodies to B- or T-cells | Is a | True | Common variable agammaglobulinemia | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR