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 |
| 15623011 | Hereditary elliptocytosis due to alpha spectrin defect | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 831282019 | Hereditary elliptocytosis due to alpha spectrin defect (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 elliptocytosis due to alpha spectrin defect | Is a | Hereditary disorder of hematologic system | false | Inferred relationship | Some | ||
| Hereditary elliptocytosis due to alpha spectrin defect | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Hereditary elliptocytosis due to alpha spectrin defect | Is a | Anaemia due to intrinsic red cell abnormality | true | Inferred relationship | Some | ||
| Hereditary elliptocytosis due to alpha spectrin defect | Is a | Hereditary elliptocytosis | true | Inferred relationship | Some | ||
| Hereditary elliptocytosis due to alpha spectrin defect | Finding site | Hematopoietic system structure | false | Inferred relationship | Some | ||
| Hereditary elliptocytosis due to alpha spectrin defect | Finding site | Erythrocyte | false | Inferred relationship | Some | 3 | |
| Hereditary elliptocytosis due to alpha spectrin defect | Finding site | Hematopoietic system structure | false | Inferred relationship | Some | ||
| Hereditary elliptocytosis due to alpha spectrin defect | Has definitional manifestation | Erythropenia | false | Inferred relationship | Some | ||
| Hereditary elliptocytosis due to alpha spectrin defect | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Hereditary elliptocytosis due to alpha spectrin defect | Has interpretation | Below reference range | true | Inferred relationship | Some | 1 | |
| Hereditary elliptocytosis due to alpha spectrin defect | Interprets | Measurement of total haemoglobin concentration | true | Inferred relationship | Some | 1 | |
| Hereditary elliptocytosis due to alpha spectrin defect | Has interpretation | Below reference range | true | Inferred relationship | Some | 2 | |
| Hereditary elliptocytosis due to alpha spectrin defect | Interprets | Red blood cell count | true | Inferred relationship | Some | 2 | |
| Hereditary elliptocytosis due to alpha spectrin defect | Has interpretation | Present | true | Inferred relationship | Some | 3 | |
| Hereditary elliptocytosis due to alpha spectrin defect | Occurrence | Congenital | true | Inferred relationship | Some | 4 | |
| Hereditary elliptocytosis due to alpha spectrin defect | Finding site | Erythrocyte | true | Inferred relationship | Some | 4 | |
| Hereditary elliptocytosis due to alpha spectrin defect | Associated morphology | Elliptocyte | true | Inferred relationship | Some | 4 | |
| Hereditary elliptocytosis due to alpha spectrin defect | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 4 | |
| Hereditary elliptocytosis due to alpha spectrin defect | Interprets | Hemolysis (observable entity) | true | Inferred relationship | Some | 3 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR