Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 293721011 | Common variable immunodeficiency with predominant immunoregulatory T-cell disorders | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 574662018 | Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 5914981000172116 | déficit immunitaire commun variable avec anomalie prédominante en lymphocytes T immunorégulateurs | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| 4551941000172118 | gewone variabele immuundeficiëntie met overwegend aandoeningen van regulerende T-cellen | nl | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| 4551951000172116 | CVID met overwegend aandoeningen van regulerende T-cellen | nl | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | Belgian module (core metadata concept) |
| 4551961000172119 | 'common variable immunodeficiency disorder' met overwegend aandoeningen van regulerende T-cellen | nl | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder) | Is a | Common variable agammaglobulinemia | false | Inferred relationship | Some | ||
| Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder) | Finding site | Structure of immune system (body structure) | true | Inferred relationship | Some | 1 | |
| Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
| Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder) | Is a | Disorder of immune structure (disorder) | false | Inferred relationship | Some | ||
| Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder) | Has definitional manifestation | Immune system finding | false | Inferred relationship | Some | ||
| Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder) | Is a | Hereditary disorder of immune system | false | Inferred relationship | Some | ||
| Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder) | Pathological process (attribute) | Abnormal immune process (qualifier value) | false | Inferred relationship | Some | 2 | |
| Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder) | Pathological process (attribute) | Abnormal immune process (qualifier value) | true | Inferred relationship | Some | 1 | |
| Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder) | Is a | Common variable immunodeficiency | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR