Status: current, Primitive. 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 | Active | Initial character case insensitive | SNOMED CT core |
574662018 | Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders | Pathological process | Abnormal immune process | true | Inferred relationship | Some | 2 | |
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders | Is a | Disorder of immune structure | true | Inferred relationship | Some | ||
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders | Has definitional manifestation | Immune system finding | false | Inferred relationship | Some | ||
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders | Is a | Common variable agammaglobulinaemia | true | Inferred relationship | Some | ||
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders | Is a | Hereditary disorder of immune system | true | Inferred relationship | Some | ||
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders | Finding site | Structure of immune system | true | Inferred relationship | Some | 1 | |
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders | Occurrence | Congenital | true | Inferred relationship | Some | 3 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set