Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1206543019 | Congenital immunodeficiency involving the haematopoietic system | en | Synonym | Active | Case insensitive | SNOMED CT core |
482175017 | Congenital immunodeficiency involving the hematopoietic system | en | Synonym | Active | Case insensitive | SNOMED CT core |
754819018 | Congenital immunodeficiency involving the hematopoietic system (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital immunodeficiency involving the haematopoietic system | Pathological process | Abnormal immune process | true | Inferred relationship | Some | 2 | |
Congenital immunodeficiency involving the haematopoietic system | Has definitional manifestation | Immune system finding | false | Inferred relationship | Some | ||
Congenital immunodeficiency involving the haematopoietic system | Is a | Congenital anomaly of the haematopoietic system | false | Inferred relationship | Some | ||
Congenital immunodeficiency involving the haematopoietic system | Is a | Congenital immunodeficiency disease | true | Inferred relationship | Some | ||
Congenital immunodeficiency involving the haematopoietic system | Finding site | Structure of immune system | false | Inferred relationship | Some | ||
Congenital immunodeficiency involving the haematopoietic system | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Congenital immunodeficiency involving the haematopoietic system | Finding site | Haematopoietic system structure | 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