Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia (disorder) | interprète (attribut) | Measurement of total haemoglobin concentration | true | Inferred relationship | Some | 2 | |
Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia (disorder) | est un(e) (attribut) | Hereditary persistence of fetal hemoglobin thalassemia | true | Inferred relationship | Some | ||
Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia (disorder) | est un(e) (attribut) | Beta plus thalassemia | true | Inferred relationship | Some | ||
Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia (disorder) | est défini par la manifestation de (attribut) | Erythropenia | false | Inferred relationship | Some | ||
Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia (disorder) | localisation d'une constatation (attribut) | structure du système hématopoïétique | false | Inferred relationship | Some | ||
Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia (disorder) | localisation d'une constatation (attribut) | structure d'un système corporel | false | Inferred relationship | Some | ||
Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia (disorder) | a pour interprétation (attribut) | au-dessous de l'étendue de référence | false | Inferred relationship | Some | 1 | |
Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia (disorder) | interprète (attribut) | Measurement of total haemoglobin concentration | false | Inferred relationship | Some | 1 | |
Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia (disorder) | a pour interprétation (attribut) | au-dessous de l'étendue de référence | true | Inferred relationship | Some | 2 | |
Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia (disorder) | interprète (attribut) | Red blood cell count | false | Inferred relationship | Some | 2 | |
Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 3 | |
Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia (disorder) | localisation d'une constatation (attribut) | Erythrocyte | true | Inferred relationship | Some | 3 | |
Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia (disorder) | localisation d'une constatation (attribut) | Erythrocyte | false | Inferred relationship | Some | ||
Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia (disorder) | localisation d'une constatation (attribut) | structure du système hématopoïétique | false | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
A>gamma< beta^+^ HPFH AND beta^0^ thalassemia in cis | est un(e) (attribut) | True | Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia (disorder) | Inferred relationship | Some |
Reference Sets
Canada English language reference set (foundation metadata concept)