Status: current, Primitive. Date: 31-Jan 2015. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3028873019 | Asplenia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3028874013 | Asplenia | en | Synonym | Active | Case insensitive | SNOMED CT core |
3028913010 | Congenital or functional absence of spleen | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Asplenia | Is a | Disorder of spleen | true | Inferred relationship | Some | ||
Asplenia | Finding site | Splenic structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Familial isolated congenital asplenia | Is a | False | Asplenia | Inferred relationship | Some | |
Bilateral right-sidedness sequence | Is a | False | Asplenia | Inferred relationship | Some | |
Functional asplenia | Is a | True | Asplenia | Inferred relationship | Some | |
Congenital absence of spleen | Is a | True | Asplenia | Inferred relationship | Some | |
Thrombocytopathy, asplenia and miosis | Is a | True | Asplenia | Inferred relationship | Some | |
Postoperative asplenia | Is a | True | Asplenia | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set