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 |
3793694018 | Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3793695017 | Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3793698015 | Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3800043011 | HPFH (hereditary persistence of fetal haemoglobin) G gamma beta plus thalassaemia | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3800044017 | HPFH (hereditary persistence of fetal hemoglobin) G gamma beta plus thalassemia | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3800045016 | HPFH (hereditary persistence of foetal haemoglobin) G gamma 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 G gamma beta plus thalassemia | Is a | Hereditary persistence of fetal hemoglobin thalassemia | true | Inferred relationship | Some | ||
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia | Is a | Beta plus thalassemia | true | Inferred relationship | Some | ||
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia | Finding site | Erythrocyte | false | Inferred relationship | Some | ||
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia | Finding site | Hematopoietic system structure | false | Inferred relationship | Some | ||
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia | Has definitional manifestation | Erythropenia | false | Inferred relationship | Some | ||
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia | Finding site | Hematopoietic system structure | false | Inferred relationship | Some | ||
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia | Finding site | Body system structure | false | Inferred relationship | Some | ||
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia | Has interpretation | Below reference range | false | Inferred relationship | Some | 1 | |
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia | Interprets | Measurement of total haemoglobin concentration | false | Inferred relationship | Some | 1 | |
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia | Has interpretation | Below reference range | true | Inferred relationship | Some | 2 | |
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia | Interprets | Red blood cell count | false | Inferred relationship | Some | 2 | |
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia | Finding site | Erythrocyte | true | Inferred relationship | Some | 3 | |
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia | 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