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 |
| 198804014 | Congenital hypergammaglobulinemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 498053010 | Congenital hypergammaglobulinaemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 796722017 | Congenital hypergammaglobulinemia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital hypergammaglobulinaemia | Is a | Congenital immunodeficiency disease | true | Inferred relationship | Some | ||
| Congenital hypergammaglobulinaemia | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Congenital hypergammaglobulinaemia | Finding site | Structure of immune system (body structure) | false | Inferred relationship | Some | ||
| Congenital hypergammaglobulinaemia | Has definitional manifestation | Immune system finding | false | Inferred relationship | Some | ||
| Congenital hypergammaglobulinaemia | Pathological process (attribute) | Abnormal immune process (qualifier value) | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Hyperimmunoglobulin E syndrome | Is a | False | Congenital hypergammaglobulinaemia | Inferred relationship | Some | |
| Hyperimmunoglobulin M syndrome | Is a | True | Congenital hypergammaglobulinaemia | Inferred relationship | Some | |
| Hyperimmunoglobulin E syndrome | Is a | True | Congenital hypergammaglobulinaemia | Inferred relationship | Some |
This concept is not in any reference sets
FHIR