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 |
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) | interprète (attribut) | Measurement of total haemoglobin concentration | true | Inferred relationship | Some | 2 | |
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) | est défini par la manifestation de (attribut) | Erythropenia | false | Inferred relationship | Some | ||
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) | localisation d'une constatation (attribut) | structure du système hématopoïétique | false | Inferred relationship | Some | ||
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) | est un(e) (attribut) | Delta beta zero thalassemia | true | Inferred relationship | Some | ||
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) | est un(e) (attribut) | Hereditary persistence of fetal hemoglobin thalassemia | true | Inferred relationship | Some | ||
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) | localisation d'une constatation (attribut) | structure d'un système corporel | false | Inferred relationship | Some | ||
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) | a pour interprétation (attribut) | au-dessous de l'étendue de référence | false | Inferred relationship | Some | 1 | |
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) | interprète (attribut) | Measurement of total haemoglobin concentration | false | Inferred relationship | Some | 1 | |
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) | a pour interprétation (attribut) | au-dessous de l'étendue de référence | true | Inferred relationship | Some | 2 | |
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) | interprète (attribut) | Red blood cell count | false | Inferred relationship | Some | 2 | |
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 3 | |
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) | localisation d'une constatation (attribut) | Erythrocyte | true | Inferred relationship | Some | 3 | |
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) | localisation d'une constatation (attribut) | structure du système hématopoïétique | false | Inferred relationship | Some | ||
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) | localisation d'une constatation (attribut) | Erythrocyte | false | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets