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 | 
| 71070019 | Congenital hemolytic anemia, NOS | en | Synonym | Inactive | Only initial character 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