Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2620662019 | Hereditary persistence of fetal hemoglobin (HPFH) A gamma beta^+^ thalassemia | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
2793326018 | Hereditary persistence of foetal haemoglobin (HPFH) A gamma beta^+^ thalassaemia | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
2914230018 | Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
2914263013 | Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3012701016 | Hereditary persistence of fetal haemoglobin A gamma beta^+^ thalassaemia | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
492143018 | HPFH A gamma beta^+^ thalassaemia | en | Synonym | Active | Case sensitive | SNOMED CT core |
66390015 | HPFH A gamma beta^+^ thalassemia | en | Synonym | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis | Is a | True | HPFH A gamma beta^+^ thalassaemia | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Australian dialect reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set