Status: current, Primitive. Date: 31-Jul 2007. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2662307010 | Hereditary hemoglobinopathy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 2674112019 | Hereditary hemoglobinopathy | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 2674113012 | Hereditary haemoglobinopathy | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary haemoglobinopathy | Is a | Haemoglobinopathy | true | Inferred relationship | Some | ||
| Hereditary haemoglobinopathy | Is a | Hereditary red blood cell disorder | true | Inferred relationship | Some | ||
| Hereditary haemoglobinopathy | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Hereditary haemoglobinopathy | Has definitional manifestation | Red blood cell finding | false | Inferred relationship | Some | ||
| Hereditary haemoglobinopathy | Finding site | Erythrocyte | false | Inferred relationship | Some | ||
| Hereditary haemoglobinopathy | Is a | Congenital disease | true | Inferred relationship | Some | ||
| Hereditary haemoglobinopathy | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Hereditary haemoglobinopathy | Finding site | Erythrocyte | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Haemoglobinopathy Toms River | Is a | True | Hereditary haemoglobinopathy | Inferred relationship | Some | |
| Homozygous hemoglobinopathy | Is a | True | Hereditary haemoglobinopathy | Inferred relationship | Some | |
| Thalassaemia | Is a | True | Hereditary haemoglobinopathy | Inferred relationship | Some | |
| Hereditary haemoglobinopathy due to globin chain mutation | Is a | True | Hereditary haemoglobinopathy | Inferred relationship | Some | |
| Hereditary persistence of fetal haemoglobin | Is a | True | Hereditary haemoglobinopathy | Inferred relationship | Some | |
| Heterozygous haemoglobinopathy | Is a | True | Hereditary haemoglobinopathy | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR