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