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 |
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