Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2015. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
71069015 | Congenital hemolytic anemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
493386016 | Congenital haemolytic anaemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
779519013 | Congenital hemolytic anemia (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Hereditary spherocytosis | Is a | False | Congenital hemolytic anemia | Inferred relationship | Existential restriction modifier | |
Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism | Is a | True | Congenital hemolytic anemia | Inferred relationship | Existential restriction modifier | |
Hereditary elliptocytosis | Is a | True | Congenital hemolytic anemia | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets