Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3439257019 | Combined immunodeficiency due to CD3gamma deficiency (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
3439258012 | Combined immunodeficiency due to CD3gamma deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3439259016 | Combined immunodeficiency due to CD3-gamma deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3439260014 | An extremely rare genetic combined primary immunodeficiency with characteristics of selective partial lymphopenia (T+/-B+NK+) phenotype and decreased CD3 complex resulting in a variable but usually mild clinical presentation ranging from asymptomatic until adulthood to high susceptibility to infections from early infancy with predominant auto-immune manifestations. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Combined immunodeficiency due to CD3-gamma deficiency | Pathological process | Abnormal immune process | true | Inferred relationship | Some | 3 | |
Combined immunodeficiency due to CD3-gamma deficiency | Is a | Autosomal recessive SCID (severe combined immunodeficiency disease) | true | Inferred relationship | Some | ||
Combined immunodeficiency due to CD3-gamma deficiency | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Combined immunodeficiency due to CD3-gamma deficiency | Finding site | Body system structure | true | Inferred relationship | Some | 2 | |
Combined immunodeficiency due to CD3-gamma deficiency | Has definitional manifestation | Immune system finding | false | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set