Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1234012018 | Stuart-Prower factor deficiency | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 127274011 | Factor X deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 3036019012 | Factor 10 deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 817385017 | Factor X deficiency (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Factor X deficiency | Interprets | Haemostatic function | true | Inferred relationship | Some | 1 | |
| Factor X deficiency | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 | |
| Factor X deficiency | Is a | Prothrombin complex deficiency | true | Inferred relationship | Some | ||
| Factor X deficiency | Is a | Coagulation factor deficiency syndrome | true | Inferred relationship | Some | ||
| Factor X deficiency | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Factor X deficiency | Has definitional manifestation | Haemostatic system finding | false | Inferred relationship | Some | ||
| Factor X deficiency | Finding site | Entire haematological system | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Factor X deficiency due to systemic amyloidosis | Is a | True | Factor X deficiency | Inferred relationship | Some | |
| Acquired factor X deficiency disease | Is a | True | Factor X deficiency | Inferred relationship | Some | |
| Hereditary factor X deficiency disease | Is a | True | Factor X deficiency | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR