Status: current, Defined. Date: 30-Apr 2022. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2787787012 | Hereditary hyperfibrinogenemia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 2791824016 | Congenital hyperfibrinogenemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 2791825015 | Hereditary hyperfibrinogenaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 2791826019 | Hereditary hyperfibrinogenemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 2795489013 | Congenital hyperfibrinogenaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary hyperfibrinogenaemia | Interprets | Haemostatic function | true | Inferred relationship | Some | 2 | |
| Hereditary hyperfibrinogenaemia | Has interpretation | Abnormal | true | Inferred relationship | Some | 2 | |
| Hereditary hyperfibrinogenaemia | Interprets | Fibrinogen assay, quantitative | true | Inferred relationship | Some | 1 | |
| Hereditary hyperfibrinogenaemia | Is a | Hereditary thrombophilia | true | Inferred relationship | Some | ||
| Hereditary hyperfibrinogenaemia | Is a | Hyperfibrinogenemia | true | Inferred relationship | Some | ||
| Hereditary hyperfibrinogenaemia | Has definitional manifestation | Fibrinogen in blood above reference range | false | Inferred relationship | Some | ||
| Hereditary hyperfibrinogenaemia | Has interpretation | Above reference range | true | Inferred relationship | Some | 1 | |
| Hereditary hyperfibrinogenaemia | Interprets | Fibrinogen measurement | false | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR