Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2612341017 | Hereditary nonspherocytic hemolytic anemia (HNSHA) due to phosphofructokinase deficiency (disorder) | en | Fully specified name | Inactive | Initial character case insensitive | SNOMED CT core |
| 2620733011 | Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to phosphofructokinase deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 2620734017 | Hereditary nonspherocytic hemolytic anemia (HNSHA) due to phosphofructokinase deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 2914229011 | Hereditary nonspherocytic hemolytic anemia due to phosphofructokinase deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 2915046010 | Hereditary nonspherocytic hemolytic anemia due to phosphofructokinase deficiency (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 3780600018 | Hereditary nonspherocytic haemolytic anaemia due to phosphofructokinase deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 69035018 | HNSHA due to phosphofructokinase deficiency | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 778169018 | HNSHA due to phosphofructokinase 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