Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2674112019 | Hereditary hemoglobinopathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2674113012 | Hereditary haemoglobinopathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5301661000241117 | hémoglobinopathie héréditaire | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary hemoglobinopathy (disorder) | Is a | Hemoglobinopathy | true | Inferred relationship | Some | ||
| Hereditary hemoglobinopathy (disorder) | Is a | Hereditary red blood cell disorder (disorder) | true | Inferred relationship | Some | ||
| Hereditary hemoglobinopathy (disorder) | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Hereditary hemoglobinopathy (disorder) | Has definitional manifestation | Red blood cell finding | false | Inferred relationship | Some | ||
| Hereditary hemoglobinopathy (disorder) | Finding site | Erythrocyte | false | Inferred relationship | Some | ||
| Hereditary hemoglobinopathy (disorder) | Is a | Congenital disease (disorder) | true | Inferred relationship | Some | ||
| Hereditary hemoglobinopathy (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Hereditary hemoglobinopathy (disorder) | Finding site | Erythrocyte | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Homozygous hemoglobinopathy | Is a | True | Hereditary hemoglobinopathy (disorder) | Inferred relationship | Some | |
| Thalassemia | Is a | True | Hereditary hemoglobinopathy (disorder) | Inferred relationship | Some | |
| Hereditary hemoglobinopathy due to globin chain mutation | Is a | True | Hereditary hemoglobinopathy (disorder) | Inferred relationship | Some | |
| Hereditary persistence of fetal hemoglobin | Is a | True | Hereditary hemoglobinopathy (disorder) | Inferred relationship | Some | |
| Heterozygous hemoglobinopathy | Is a | True | Hereditary hemoglobinopathy (disorder) | Inferred relationship | Some | |
| Haemoglobinopathy Toms River | Is a | True | Hereditary hemoglobinopathy (disorder) | Inferred relationship | Some |
This concept is not in any reference sets
FHIR