Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3793710015 | Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3793711016 | Hereditary persistence of fetal hemoglobin delta beta plus thalassemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
3793712011 | Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
3793714012 | Hereditary persistence of foetal haemoglobin delta beta plus thalassaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
3793721012 | HPFH (hereditary persistence of fetal hemoglobin) delta beta plus thalassemia | en | Synonym | Active | Case sensitive | SNOMED CT core |
3793726019 | HPFH (hereditary persistence of fetal haemoglobin) delta beta plus thalassaemia | en | Synonym | Active | Case sensitive | SNOMED CT core |
3793727011 | HPFH (hereditary persistence of foetal haemoglobin) delta beta plus thalassaemia | en | Synonym | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia | Interprets | Measurement of total haemoglobin concentration | true | Inferred relationship | Some | 2 | |
Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia | Has definitional manifestation | Erythropenia | false | Inferred relationship | Some | ||
Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia | Finding site | Haematopoietic system structure | false | Inferred relationship | Some | ||
Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia | Is a | Delta beta zero thalassaemia | true | Inferred relationship | Some | ||
Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia | Is a | Hereditary persistence of fetal haemoglobin thalassaemia | true | Inferred relationship | Some | ||
Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia | Finding site | Body system structure | false | Inferred relationship | Some | ||
Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia | Has interpretation | Below reference range | false | Inferred relationship | Some | 1 | |
Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia | Interprets | Measurement of total haemoglobin concentration | false | Inferred relationship | Some | 1 | |
Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia | Has interpretation | Below reference range | true | Inferred relationship | Some | 2 | |
Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia | Interprets | Red blood cell count | false | Inferred relationship | Some | 2 | |
Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia | Finding site | Erythrocyte | true | Inferred relationship | Some | 3 | |
Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia | Finding site | Haematopoietic system structure | false | Inferred relationship | Some | ||
Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia | Finding site | Erythrocyte | false | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set