Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Dec 2024. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5420180016 | Autosomal dominant combined variable immunodeficiency due to TWEAK deficiency | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 5420181017 | Autosomal dominant combined variable immunodeficiency due to TWEAK mutation | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 5420182012 | Autosomal dominant combined variable immunodeficiency due to tumor necrosis factor-like weak inducer of apoptosis mutation (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5420183019 | Autosomal dominant combined variable immunodeficiency due to tumour necrosis factor-like weak inducer of apoptosis mutation | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5420184013 | Autosomal dominant combined variable immunodeficiency due to tumor necrosis factor-like weak inducer of apoptosis mutation | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5420185014 | Autosomal dominant CVID (combined variable immunodeficiency) due to TNFSF12 mutation | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Autosomal dominant combined variable immunodeficiency due to TWEAK mutation | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Autosomal dominant combined variable immunodeficiency due to TWEAK mutation | Is a | Common variable immunodeficiency | true | Inferred relationship | Some | ||
| Autosomal dominant combined variable immunodeficiency due to TWEAK mutation | Is a | Hereditary disorder of immune system | true | Inferred relationship | Some | ||
| Autosomal dominant combined variable immunodeficiency due to TWEAK mutation | Finding site | Structure of immune system (body structure) | true | Inferred relationship | Some | 1 | |
| Autosomal dominant combined variable immunodeficiency due to TWEAK mutation | Pathological process (attribute) | Abnormal immune process (qualifier value) | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR