Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
10925016 | A>gamma< beta^+^ HPFH AND beta^0^ thalassemia in cis | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
498509010 | A>gamma< beta^+^ HPFH AND beta^0^ thalassaemia in cis | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
2988972011 | A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis (disorder) | en | Fully specified name | Active | Entire term case sensitive | SNOMED CT core module |
3023237017 | A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis | Is a | Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia | true | Inferred relationship | Existential restriction modifier | ||
A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis | Finding site | Hematopoietic system structure | false | Inferred relationship | Existential restriction modifier | ||
A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis | Finding site | Erythrocyte | false | Inferred relationship | Existential restriction modifier | ||
A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis | Has definitional manifestation | Erythropenia | false | Inferred relationship | Existential restriction modifier | ||
A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis | Finding site | Hematopoietic system structure | false | Inferred relationship | Existential restriction modifier | ||
A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier | ||
A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis | Has interpretation | Below reference range | false | Inferred relationship | Existential restriction modifier | 1 | |
A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis | Interprets | Measurement of total hemoglobin concentration | false | Inferred relationship | Existential restriction modifier | 1 | |
A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis | Has interpretation | Below reference range | true | Inferred relationship | Existential restriction modifier | 2 | |
A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis | Interprets | Red blood cell count | false | Inferred relationship | Existential restriction modifier | 2 | |
A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 3 | |
A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis | Finding site | Erythrocyte | true | Inferred relationship | Existential restriction modifier | 3 | |
A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis | Interprets | Measurement of total hemoglobin concentration | true | Inferred relationship | Existential restriction modifier | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets