Status: current, Primitive. Date: 31-Jul 2003. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1782839018 | X-linked hyper-IgM syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 1787887015 | X-linked with hyper-IgM immunodeficiency | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 2970489019 | X-linked hyper-immunoglobulin M syndrome (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
| 2970494019 | X-linked hyper-immunoglobulin M syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| X-linked hyper-IgM syndrome | Pathological process | Abnormal immune process | true | Inferred relationship | Some | 2 | |
| X-linked hyper-IgM syndrome | Is a | X-linked recessive hereditary disease | true | Inferred relationship | Some | ||
| X-linked hyper-IgM syndrome | Is a | Hyper IgM syndrome | true | Inferred relationship | Some | ||
| X-linked hyper-IgM syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| X-linked hyper-IgM syndrome | Finding site | Structure of immune system | false | Inferred relationship | Some | ||
| X-linked hyper-IgM syndrome | Has definitional manifestation | Immune system finding | false | Inferred relationship | Some | ||
| X-linked hyper-IgM syndrome | Is a | X-linked hereditary disease | 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