Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 351575018 | Deletion of X-chromosome and hypogammaglobulinemia | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 351576017 | Deletion of X-chromosome and hypogammaglobulinaemia | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 622984017 | Deletion of X-chromosome and hypogammaglobulinemia (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Deletion of X-chromosome and hypogammaglobulinaemia | Pathological process | Abnormal immune process | true | Inferred relationship | Some | 3 | |
| Deletion of X-chromosome and hypogammaglobulinaemia | Is a | Disorder of immune structure | true | Inferred relationship | Some | ||
| Deletion of X-chromosome and hypogammaglobulinaemia | Associated with | Chromosomal disorder | true | Inferred relationship | Some | 2 | |
| Deletion of X-chromosome and hypogammaglobulinaemia | Has definitional manifestation | Immune system finding | false | Inferred relationship | Some | ||
| Deletion of X-chromosome and hypogammaglobulinaemia | Is a | Immunodeficiency associated with chromosomal abnormality | true | Inferred relationship | Some | ||
| Deletion of X-chromosome and hypogammaglobulinaemia | Finding site | Structure of immune system | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR