Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 351296012 | Combined coagulation factor deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 622786010 | Combined coagulation factor deficiency (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Combined coagulation factor deficiency | Interprets | Haemostatic function | true | Inferred relationship | Some | 1 | |
| Combined coagulation factor deficiency | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 | |
| Combined coagulation factor deficiency | Is a | Coagulation factor deficiency syndrome | true | Inferred relationship | Some | ||
| Combined coagulation factor deficiency | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Combined coagulation factor deficiency | Has definitional manifestation | Haemostatic system finding | false | Inferred relationship | Some | ||
| Combined coagulation factor deficiency | Is a | Blood coagulation disorder | false | Inferred relationship | Some | ||
| Combined coagulation factor deficiency | Finding site | Entire haematological system | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Familial multiple factor deficiency syndrome | Is a | True | Combined coagulation factor deficiency | Inferred relationship | Some | |
| Hereditary combined coagulation factor deficiency | Is a | True | Combined coagulation factor deficiency | Inferred relationship | Some | |
| Acquired combined coagulation factor deficiency | Is a | True | Combined coagulation factor deficiency | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR