Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2620625016 | Severe combined immunodeficiency (SCID) due to absent peripheral T cell maturation | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 2913244019 | Severe combined immunodeficiency due to absent peripheral T cell maturation | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 2914606012 | Severe combined immunodeficiency due to absent peripheral T cell maturation (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
| 485833013 | Combined immunodeficiency associated with maturation pathway defect | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 6812016 | SCID due to absent peripheral T cell maturation | en | Synonym | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| SCID due to absent peripheral T cell maturation | Pathological process | Abnormal immune process | true | Inferred relationship | Some | 3 | |
| SCID due to absent peripheral T cell maturation | Is a | Severe combined immunodeficiency disease | true | Inferred relationship | Some | ||
| SCID due to absent peripheral T cell maturation | Finding site | Body system structure | true | Inferred relationship | Some | 1 | |
| SCID due to absent peripheral T cell maturation | Has definitional manifestation | Immune system finding | false | Inferred relationship | Some | ||
| SCID due to absent peripheral T cell maturation | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
| SCID due to absent peripheral T cell maturation | Finding site | Structure of immune system | false | Inferred relationship | Some | ||
| SCID due to absent peripheral T cell maturation | Severity | Severe | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Severe combined immunodeficiency with reticular dysgenesis | Is a | True | SCID due to absent peripheral T cell maturation | Inferred relationship | Some | |
| Reticular dysgenesis | Is a | True | SCID due to absent peripheral T cell maturation | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR