Status: current, Primitive. Date: 31-Jan 2009. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2787558013 | Hereditary combined coagulation factor deficiency (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 2795244014 | Hereditary combined coagulation factor deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary combined coagulation factor deficiency | Interprets | Haemostatic function | true | Inferred relationship | Some | 1 | |
| Hereditary combined coagulation factor deficiency | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 | |
| Hereditary combined coagulation factor deficiency | Is a | Hereditary coagulation factor deficiency | true | Inferred relationship | Some | ||
| Hereditary combined coagulation factor deficiency | Is a | Combined coagulation factor deficiency | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Combined deficiency of factor V and factor VIII | Is a | True | Hereditary combined coagulation factor deficiency | Inferred relationship | Some | |
| Hereditary combined deficiency of vitamin K-dependent clotting factors | Is a | True | Hereditary combined coagulation factor deficiency | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR