Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2005. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module | 
| 70881014 | HNSHA due to hexokinase deficiency | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module | 
| 70882019 | Hexokinase deficiency anemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module | 
| 493331017 | Hexokinase deficiency anaemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module | 
| 779388011 | HNSHA due to hexokinase deficiency (disorder) | en | Fully specified name | Inactive | Entire term case sensitive | SNOMED CT core module | 
| 2612393015 | Hereditary nonspherocytic hemolytic anemia (HNSHA) due to hexokinase deficiency (disorder) | en | Fully specified name | Inactive | Only initial character case insensitive | SNOMED CT core module | 
| 2620808016 | Hereditary nonspherocytic hemolytic anemia (HNSHA) due to hexokinase deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module | 
| 2620809012 | Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to hexokinase deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module | 
| 2913911019 | Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module | 
| 2914854018 | Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module | 
| 3780592013 | Hereditary nonspherocytic haemolytic anaemia due to hexokinase deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module | 
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
This concept is not in any reference sets