Status: current, Primitive. Date: 31-Jan 2009. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2789153017 | Hyperfibrinogenemia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 2793786017 | Hyperfibrinogenaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 2795467014 | Hyperfibrinogenemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hyperfibrinogenemia | Interprets | Haemostatic function | true | Inferred relationship | Some | 2 | |
| Hyperfibrinogenemia | Has interpretation | Abnormal | true | Inferred relationship | Some | 2 | |
| Hyperfibrinogenemia | Interprets | Fibrinogen assay, quantitative | false | Inferred relationship | Some | 1 | |
| Hyperfibrinogenemia | Is a | Fibrinogen abnormality | true | Inferred relationship | Some | ||
| Hyperfibrinogenemia | Has definitional manifestation | Fibrinogen in blood above reference range | false | Inferred relationship | Some | ||
| Hyperfibrinogenemia | Has interpretation | Above reference range | true | Inferred relationship | Some | 1 | |
| Hyperfibrinogenemia | Is a | Fibrinogen in blood above reference range | true | Inferred relationship | Some | ||
| Hyperfibrinogenemia | Interprets | Fibrinogen measurement | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Hereditary hyperfibrinogenaemia | Is a | True | Hyperfibrinogenemia | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR