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