Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 293705018 | Severe combined immunodeficiency with low T- and B-cell numbers | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 574645011 | Severe combined immunodeficiency with low T- and B-cell numbers (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Severe combined immunodeficiency with low T- and B-cell numbers | Pathological process | Abnormal immune process | true | Inferred relationship | Some | 3 | |
| Severe combined immunodeficiency with low T- and B-cell numbers | Is a | Disorder of immune structure | true | Inferred relationship | Some | ||
| Severe combined immunodeficiency with low T- and B-cell numbers | Has definitional manifestation | Immune system finding | false | Inferred relationship | Some | ||
| Severe combined immunodeficiency with low T- and B-cell numbers | Is a | Severe combined immunodeficiency disease | true | Inferred relationship | Some | ||
| Severe combined immunodeficiency with low T- and B-cell numbers | Severity | Severe | false | Inferred relationship | Some | ||
| Severe combined immunodeficiency with low T- and B-cell numbers | Finding site | Structure of immune system | true | Inferred relationship | Some | 1 | |
| Severe combined immunodeficiency with low T- and B-cell numbers | Occurrence | Congenital | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Severe combined immunodeficiency due to LCK deficiency | Is a | True | Severe combined immunodeficiency with low T- and B-cell numbers | Inferred relationship | Some | |
| Short-limb skeletal dysplasia with severe combined immunodeficiency | Is a | True | Severe combined immunodeficiency with low T- and B-cell numbers | Inferred relationship | Some | |
| Hepatic veno-occlusive disease with immunodeficiency syndrome | Is a | True | Severe combined immunodeficiency with low T- and B-cell numbers | Inferred relationship | Some | |
| Cernunnos-XLF deficiency | Is a | True | Severe combined immunodeficiency with low T- and B-cell numbers | Inferred relationship | Some | |
| Omenn syndrome | Is a | True | Severe combined immunodeficiency with low T- and B-cell numbers | Inferred relationship | Some | |
| Severe combined immunodeficiency due to CTPS1 deficiency | Is a | True | Severe combined immunodeficiency with low T- and B-cell numbers | Inferred relationship | Some | |
| Severe combined immunodeficiency due to complete RAG1 and/or RAG2 deficiency | Is a | True | Severe combined immunodeficiency with low T- and B-cell numbers | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR