Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2532304011 | Immunodeficiency associated with 18p syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 351583012 | 18-p syndrome with associated immunodeficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 622987012 | 18-p syndrome with associated immunodeficiency (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Immunodeficiency associated with 18p syndrome | Pathological process | Abnormal immune process | true | Inferred relationship | Some | 2 | |
| Immunodeficiency associated with 18p syndrome | Has definitional manifestation | Immune system finding | false | Inferred relationship | Some | ||
| Immunodeficiency associated with 18p syndrome | Associated with | Chromosomal disorder | true | Inferred relationship | Some | 1 | |
| Immunodeficiency associated with 18p syndrome | Is a | Immunodeficiency associated with chromosomal abnormality | true | Inferred relationship | Some | ||
| Immunodeficiency associated with 18p syndrome | Finding site | Structure of immune system | false | Inferred relationship | Some |
| 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