Status: current, Primitive. Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3760130017 | Combined immunodeficiency with granulomatosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3760131018 | Combined immunodeficiency due to RAG 1/2 deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 3760132013 | Combined immunodeficiency with granulomatosis (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 3760133015 | Combined immunodeficiency due to RAG 1/2 (recombination activating gene 1/2) deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 3760136011 | A rare genetic non-severe combined immunodeficiency disease with characteristics of immunodeficiency (manifested by recurrent and/or severe bacterial and viral infections), destructive noninfectious granulomas involving skin, mucosa and internal organs and various autoimmune manifestations (including cytopenia, vitiligo, psoriasis, myasthenia gravis, enteropathy). Immunophenotypically, T-cell and B-cell lymphopenia, hypogammaglobulinaemia, abnormal specific antibody production and impaired T-cell function are observed. | en | Definition | Active | Case sensitive | SNOMED CT core |
| 3760137019 | A rare genetic non-severe combined immunodeficiency disease with characteristics of immunodeficiency (manifested by recurrent and/or severe bacterial and viral infections), destructive noninfectious granulomas involving skin, mucosa and internal organs and various autoimmune manifestations (including cytopenia, vitiligo, psoriasis, myasthenia gravis, enteropathy). Immunophenotypically, T-cell and B-cell lymphopenia, hypogammaglobulinemia, abnormal specific antibody production and impaired T-cell function are observed. | en | Definition | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Combined immunodeficiency with granulomatosis | Is a | Combined immunodeficiency disease | true | Inferred relationship | Some | ||
| Combined immunodeficiency with granulomatosis | Is a | Genetic disease | true | Inferred relationship | Some | ||
| Combined immunodeficiency with granulomatosis | Is a | Granulomatosis | true | Inferred relationship | Some | ||
| Combined immunodeficiency with granulomatosis | Pathological process | Abnormal immune process | true | Inferred relationship | Some | 2 | |
| Combined immunodeficiency with granulomatosis | Associated morphology | Granulomatosis | 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