Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
89768011 | HPFH delta beta^0^ thalassemia | en | Synonym (core metadata concept) | Inactive | Entire term case sensitive (core metadata concept) | SNOMED CT core |
496831019 | HPFH delta beta^0^ thalassaemia | en | Synonym (core metadata concept) | Inactive | Entire term case sensitive (core metadata concept) | SNOMED CT core |
792190012 | HPFH delta beta^0^ thalassemia (disorder) | en | Fully specified name | Inactive | Entire term case sensitive (core metadata concept) | SNOMED CT core |
2612423014 | Hereditary persistence of fetal hemoglobin (HPFH) delta beta^0^ thalassemia (disorder) | en | Fully specified name | Inactive | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
2620864016 | Hereditary persistence of fetal hemoglobin (HPFH) delta beta^0^ thalassemia | en | Synonym (core metadata concept) | Inactive | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
2620865015 | Hereditary persistence of fetal haemoglobin (HPFH) delta beta^0^ thalassaemia | en | Synonym (core metadata concept) | Inactive | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
2793507013 | Hereditary persistence of foetal haemoglobin (HPFH) delta beta^0^ thalassaemia | en | Synonym (core metadata concept) | Inactive | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
2914025011 | Hereditary persistence of fetal hemoglobin delta beta^0^ thalassemia | en | Synonym (core metadata concept) | Inactive | Entire term case insensitive (core metadata concept) | SNOMED CT core |
2915272012 | Hereditary persistence of fetal hemoglobin delta beta^0^ thalassemia (disorder) | en | Fully specified name | Inactive | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3014106018 | Hereditary persistence of fetal haemoglobin delta beta^0^ thalassaemia | en | Synonym (core metadata concept) | Inactive | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3793710015 | Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3793711016 | Hereditary persistence of fetal hemoglobin delta beta plus thalassemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3793712011 | Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3793714012 | Hereditary persistence of foetal haemoglobin delta beta plus thalassaemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3793721012 | HPFH (hereditary persistence of fetal hemoglobin) delta beta plus thalassemia | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3793726019 | HPFH (hereditary persistence of fetal haemoglobin) delta beta plus thalassaemia | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3793727011 | HPFH (hereditary persistence of foetal haemoglobin) delta beta plus thalassaemia | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) | Is a | Delta beta zero thalassemia | true | Inferred relationship | Some | ||
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) | Is a | Hereditary persistence of fetal hemoglobin thalassemia | true | Inferred relationship | Some | ||
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) | Finding site | Hematopoietic system structure | false | Inferred relationship | Some | ||
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) | Finding site | Erythrocyte | false | Inferred relationship | Some | ||
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) | Has definitional manifestation | Erythropenia | false | Inferred relationship | Some | ||
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) | Finding site | Hematopoietic system structure | false | Inferred relationship | Some | ||
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) | Finding site | Body system structure | false | Inferred relationship | Some | ||
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) | Has interpretation | Below reference range | false | Inferred relationship | Some | 1 | |
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) | Interprets | Measurement of total haemoglobin concentration | false | Inferred relationship | Some | 1 | |
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) | Has interpretation | Below reference range | true | Inferred relationship | Some | 2 | |
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) | Interprets | Red blood cell count | false | Inferred relationship | Some | 2 | |
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) | Finding site | Erythrocyte | true | Inferred relationship | Some | 3 | |
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) | Interprets | Measurement of total haemoglobin concentration | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets