Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 198804014 | Congenital hypergammaglobulinemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 498053010 | Congenital hypergammaglobulinaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 796722017 | Congenital hypergammaglobulinemia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital hypergammaglobulinaemia | Pathological process | Abnormal immune process | true | Inferred relationship | Some | 2 | |
| Congenital hypergammaglobulinaemia | Is a | Congenital immunodeficiency disease | true | Inferred relationship | Some | ||
| Congenital hypergammaglobulinaemia | Has definitional manifestation | Immune system finding | false | Inferred relationship | Some | ||
| Congenital hypergammaglobulinaemia | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Congenital hypergammaglobulinaemia | Finding site | Structure of immune system | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Hyperimmunoglobulin E syndrome | Is a | False | Congenital hypergammaglobulinaemia | Inferred relationship | Some | |
| Hyper IgM syndrome | Is a | True | Congenital hypergammaglobulinaemia | Inferred relationship | Some | |
| Autosomal dominant hyper-IgE syndrome | Is a | True | Congenital hypergammaglobulinaemia | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR