Status: current, Defined. Date: 31-Jan 2005. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2612393015 | Hereditary nonspherocytic hemolytic anemia (HNSHA) due to hexokinase deficiency (disorder) | en | Fully specified name | Inactive | Initial character case insensitive | SNOMED CT core |
| 2620808016 | Hereditary nonspherocytic hemolytic anemia (HNSHA) due to hexokinase deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 2620809012 | Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to hexokinase deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 2913911019 | Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 2914854018 | Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3780592013 | Hereditary nonspherocytic haemolytic anaemia due to hexokinase deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 493331017 | Hexokinase deficiency anaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 70881014 | HNSHA due to hexokinase deficiency | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 70882019 | Hexokinase deficiency anemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 779388011 | HNSHA due to hexokinase deficiency (disorder) | en | Fully specified name | Inactive | Case sensitive | SNOMED CT core |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set