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 |
| 326013 | Hereditary hemoglobinopathy due to globin chain mutation | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 206335017 | Structural hemoglobinopathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 474018017 | Hereditary haemoglobinopathy due to globin chain mutation | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 474019013 | Structural haemoglobinopathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 731076011 | Hereditary hemoglobinopathy due to globin chain mutation (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary hemoglobinopathy due to globin chain mutation | Is a | Hemoglobinopathy | false | Inferred relationship | Some | ||
| Hereditary hemoglobinopathy due to globin chain mutation | Finding site | Hematopoietic system structure | false | Inferred relationship | Some | ||
| Hereditary hemoglobinopathy due to globin chain mutation | Finding site | Erythrocyte | false | Inferred relationship | Some | ||
| Hereditary hemoglobinopathy due to globin chain mutation | Finding site | Hematopoietic system structure | false | Inferred relationship | Some | ||
| Hereditary hemoglobinopathy due to globin chain mutation | Is a | Hereditary red blood cell disorder (disorder) | false | Inferred relationship | Some | ||
| Hereditary hemoglobinopathy due to globin chain mutation | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Hereditary hemoglobinopathy due to globin chain mutation | Has definitional manifestation | Red blood cell finding | false | Inferred relationship | Some | ||
| Hereditary hemoglobinopathy due to globin chain mutation | Is a | Hereditary hemoglobinopathy (disorder) | true | Inferred relationship | Some | ||
| Hereditary hemoglobinopathy due to globin chain mutation | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Hereditary hemoglobinopathy due to globin chain mutation | Finding site | Erythrocyte | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Unstable hemoglobin disease | Is a | True | Hereditary hemoglobinopathy due to globin chain mutation | Inferred relationship | Some | |
| Hemoglobin E disease | Is a | True | Hereditary hemoglobinopathy due to globin chain mutation | Inferred relationship | Some | |
| Hemoglobin E trait | Is a | True | Hereditary hemoglobinopathy due to globin chain mutation | Inferred relationship | Some | |
| Hemoglobin C disease | Is a | True | Hereditary hemoglobinopathy due to globin chain mutation | Inferred relationship | Some | |
| Hemoglobin D disease | Is a | True | Hereditary hemoglobinopathy due to globin chain mutation | Inferred relationship | Some | |
| Hemoglobin D trait | Is a | True | Hereditary hemoglobinopathy due to globin chain mutation | Inferred relationship | Some | |
| Hemoglobin M disease | Is a | True | Hereditary hemoglobinopathy due to globin chain mutation | Inferred relationship | Some | |
| Hemoglobin C trait | Is a | True | Hereditary hemoglobinopathy due to globin chain mutation | Inferred relationship | Some | |
| Hereditary hemoglobin S (disorder) | Is a | True | Hereditary hemoglobinopathy due to globin chain mutation | Inferred relationship | Some | |
| Congenital methemoglobinemia with abnormal methemoglobins | Is a | True | Hereditary hemoglobinopathy due to globin chain mutation | Inferred relationship | Some | |
| Hemoglobin O-Arab trait (disorder) | Is a | True | Hereditary hemoglobinopathy due to globin chain mutation | Inferred relationship | Some |
This concept is not in any reference sets
FHIR