Status: current, 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 |
| 482275013 | Hereditary disorder of immune system | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 754928016 | Hereditary disorder of immune system (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 |
| Hereditary disorder of immune system | Is a | Disorder of immune system | false | Inferred relationship | Some | ||
| Hereditary disorder of immune system | Is a | Hereditary disorder by system | true | Inferred relationship | Some | ||
| Hereditary disorder of immune system | Finding site | Structure of immune system (body structure) | false | Inferred relationship | Some | ||
| Hereditary disorder of immune system | Is a | Disorder of immune function (disorder) | true | Inferred relationship | Some | ||
| Hereditary disorder of immune system | Finding site | Body system structure | true | Inferred relationship | Some | 1 | |
| Hereditary disorder of immune system | Has definitional manifestation | Immune system finding | false | Inferred relationship | Some | ||
| Hereditary disorder of immune system | Pathological process (attribute) | Abnormal immune process (qualifier value) | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Keratitis fugax hereditaria | Is a | True | Hereditary disorder of immune system | Inferred relationship | Some | |
| Developmental delay, immunodeficiency, leukoencephalopathy, hypohomocysteinemia syndrome | Is a | True | Hereditary disorder of immune system | Inferred relationship | Some | |
| Autosomal recessive hyper-IgE syndrome due to ZNF341 deficiency | Is a | True | Hereditary disorder of immune system | Inferred relationship | Some |
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This concept is not in any reference sets
FHIR