Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3663200016 | Genetic hyperferritinemia without iron overload | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3663201017 | Benign hyperferritinemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3663202012 | Genetic hyperferritinemia without iron overload (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3663203019 | A rare biological anomaly defined as high serum ferritin levels without elevations of transferrin saturation, tissue or serum iron and with characteristics of an apparently asymptomatic clinical phenotype. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Genetic hyperferritinemia without iron overload | Is a | Serum ferritin above reference range | true | Inferred relationship | Some | ||
| Genetic hyperferritinemia without iron overload | Has interpretation | Above reference range | true | Inferred relationship | Some | 1 | |
| Genetic hyperferritinemia without iron overload | Interprets | Serum ferritin measurement | true | Inferred relationship | Some | 1 | |
| Genetic hyperferritinemia without iron overload | Is a | Autosomal hereditary disorder | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR