Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1225271012 | Fitzgerald-Flaujeac-Williams-Reid trait | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 45657014 | High molecular weight kininogen deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 45658016 | Fitzgerald factor deficiency | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 757865012 | High molecular weight kininogen deficiency (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| High molecular weight kininogen deficiency | Interprets | Haemostatic function | true | Inferred relationship | Some | 1 | |
| High molecular weight kininogen deficiency | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 | |
| High molecular weight kininogen deficiency | Is a | Contact factor deficiency | true | Inferred relationship | Some | ||
| High molecular weight kininogen deficiency | Is a | Coagulation factor deficiency syndrome | true | Inferred relationship | Some | ||
| High molecular weight kininogen deficiency | Finding site | Body system structure | false | Inferred relationship | Some | ||
| High molecular weight kininogen deficiency | Has definitional manifestation | Haemostatic system finding | false | Inferred relationship | Some | ||
| High molecular weight kininogen deficiency | Finding site | Entire haematological system | false | Inferred relationship | Some |
| 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