Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 178844010 | Dysfibrinogenemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 189812014 | Dysfibrinogenemia, NOS | en | Synonym | Inactive | Initial character case insensitive | SNOMED CT core |
| 363901010 | Dysfibrinogenaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 632834017 | Dysfibrinogenemia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Dysfibrinogenaemia | Interprets | Haemostatic function | true | Inferred relationship | Some | 1 | |
| Dysfibrinogenaemia | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 | |
| Dysfibrinogenaemia | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
| Dysfibrinogenaemia | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Dysfibrinogenaemia | Has definitional manifestation | Haemostatic system finding | false | Inferred relationship | Some | ||
| Dysfibrinogenaemia | Is a | Factor I deficiency disease | true | Inferred relationship | Some | ||
| Dysfibrinogenaemia | Finding site | Entire haematological system | false | Inferred relationship | Some | ||
| Dysfibrinogenaemia | Is a | Congenital fibrinogen abnormality | true | Inferred relationship | Some | ||
| Dysfibrinogenaemia | Is a | Coagulation factor deficiency syndrome | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Hereditary dysfibrinogenaemia | Is a | True | Dysfibrinogenaemia | Inferred relationship | Some | |
| Alpha chain defect dysfibrinogenaemia | Is a | True | Dysfibrinogenaemia | Inferred relationship | Some | |
| Beta chain defect dysfibrinogenaemia | Is a | True | Dysfibrinogenaemia | Inferred relationship | Some | |
| Gamma chain defect dysfibrinogenaemia | Is a | True | Dysfibrinogenaemia | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR