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 |
28713012 | Hereditary persistence of fetal hemoglobin thalassemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
478010018 | Hereditary persistence of fetal haemoglobin thalassaemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
744092016 | Hereditary persistence of fetal hemoglobin thalassemia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
2793345010 | Hereditary persistence of foetal haemoglobin thalassaemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5244049012 | HPFH (hereditary persistence of fetal haemoglobin) beta-thalassaemia syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5244050012 | HPFH (hereditary persistence of fetal hemoglobin) beta-thalassemia syndrome | 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 thalassemia | Is a | Thalassemia | true | Inferred relationship | Some | ||
Hereditary persistence of fetal hemoglobin thalassemia | Finding site | Erythrocyte | false | Inferred relationship | Some | ||
Hereditary persistence of fetal hemoglobin thalassemia | Finding site | Hematopoietic system structure | false | Inferred relationship | Some | ||
Hereditary persistence of fetal hemoglobin thalassemia | Finding site | Hematopoietic system structure | false | Inferred relationship | Some | ||
Hereditary persistence of fetal hemoglobin thalassemia | Has definitional manifestation | Erythropenia | false | Inferred relationship | Some | ||
Hereditary persistence of fetal hemoglobin thalassemia | Finding site | Body system structure | false | Inferred relationship | Some | ||
Hereditary persistence of fetal hemoglobin thalassemia | Has interpretation | Below reference range | false | Inferred relationship | Some | 1 | |
Hereditary persistence of fetal hemoglobin thalassemia | Interprets | Measurement of total haemoglobin concentration | false | Inferred relationship | Some | 1 | |
Hereditary persistence of fetal hemoglobin thalassemia | Has interpretation | Below reference range | true | Inferred relationship | Some | 2 | |
Hereditary persistence of fetal hemoglobin thalassemia | Interprets | Red blood cell count | false | Inferred relationship | Some | 2 | |
Hereditary persistence of fetal hemoglobin thalassemia | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
Hereditary persistence of fetal hemoglobin thalassemia | Finding site | Erythrocyte | true | Inferred relationship | Some | 3 | |
Hereditary persistence of fetal hemoglobin thalassemia | Interprets | Measurement of total haemoglobin concentration | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
HPFH unlinked to beta-globulin gene cluster | Is a | True | Hereditary persistence of fetal hemoglobin thalassemia | Inferred relationship | Some | |
HPFH A gamma beta^+^ thalassemia | Is a | True | Hereditary persistence of fetal hemoglobin thalassemia | Inferred relationship | Some | |
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) | Is a | True | Hereditary persistence of fetal hemoglobin thalassemia | Inferred relationship | Some | |
HPFH nondeletion type | Is a | True | Hereditary persistence of fetal hemoglobin thalassemia | Inferred relationship | Some | |
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia | Is a | True | Hereditary persistence of fetal hemoglobin thalassemia | Inferred relationship | Some | |
HPFH deletion type | Is a | True | Hereditary persistence of fetal hemoglobin thalassemia | Inferred relationship | Some | |
HPFH linked to beta-globulin gene cluster | Is a | True | Hereditary persistence of fetal hemoglobin thalassemia | Inferred relationship | Some |
This concept is not in any reference sets