Status: current, Defined. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
153877013 | Congenital absence of spleen | en | Synonym | Active | Case insensitive | SNOMED CT core |
153878015 | Congenital asplenia | en | Synonym | Active | Case insensitive | SNOMED CT core |
836678011 | Congenital absence of spleen (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Agenesis of spleen | Is a | True | Congenital absence of spleen | Inferred relationship | Some | |
Diaphragmatic hernia, short bowel, asplenia syndrome | Is a | True | Congenital absence of spleen | Inferred relationship | Some | |
Functional asplenia | Is a | False | Congenital absence of spleen | Inferred relationship | Some | |
Bilateral right-sidedness sequence | Is a | False | Congenital absence of spleen | Inferred relationship | Some | |
Familial isolated congenital asplenia | Is a | True | Congenital absence of spleen | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set