Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1230410010 | Factor XII deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 1230411014 | Hageman factor deficiency | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 78295019 | Factor XII deficiency disease | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 784389014 | Factor XII deficiency disease (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Factor XII deficiency disease | Interprets | Haemostatic function | true | Inferred relationship | Some | 1 | |
| Factor XII deficiency disease | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 | |
| Factor XII deficiency disease | Is a | Contact factor deficiency | true | Inferred relationship | Some | ||
| Factor XII deficiency disease | Is a | Coagulation factor deficiency syndrome | true | Inferred relationship | Some | ||
| Factor XII deficiency disease | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Factor XII deficiency disease | Has definitional manifestation | Haemostatic system finding | false | Inferred relationship | Some | ||
| Factor XII deficiency disease | Finding site | Entire haematological system | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Acquired factor XII deficiency disease | Is a | True | Factor XII deficiency disease | Inferred relationship | Some | |
| Hereditary factor XII deficiency disease | Is a | True | Factor XII deficiency disease | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR