Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 153877013 | Congenital absence of spleen | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 153878015 | Congenital asplenia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 836678011 | Congenital absence of spleen (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 1235779019 | Splenic agenesis | en | Synonym | Inactive | Entire term case insensitive | SNOMED CT core module |
| 1235780016 | Splenic aplasia | en | Synonym | Inactive | Only initial character case insensitive | SNOMED CT core module |
| 215631000000118 | Asplenia | en | Synonym | Inactive | Only initial character case insensitive | SNOMED CT United Kingdom Edition module |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Functional asplenia | Is a | False | Congenital absence of spleen | Inferred relationship | Existential restriction modifier | |
| Bilateral right-sidedness sequence | Is a | False | Congenital absence of spleen | Inferred relationship | Existential restriction modifier | |
| Familial isolated congenital asplenia | Is a | True | Congenital absence of spleen | Inferred relationship | Existential restriction modifier | |
| Agenesis of spleen | Is a | True | Congenital absence of spleen | Inferred relationship | Existential restriction modifier | |
| Diaphragmatic hernia, short bowel, asplenia syndrome | Is a | True | Congenital absence of spleen | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets