Status: current, Primitive. Date: 31-Jan 2009. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2788203011 | Factor I deficiency disease (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
| 2792737011 | Factor I deficiency disease | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 2884951017 | Disease that manifests either a quantitative or a qualitative defect of factor I | en | Definition | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Factor I deficiency disease | Interprets | Haemostatic function | true | Inferred relationship | Some | 1 | |
| Factor I deficiency disease | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 | |
| Factor I deficiency disease | Is a | Coagulation factor deficiency syndrome | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Hypofibrinogenaemia | Is a | True | Factor I deficiency disease | Inferred relationship | Some | |
| Dysfibrinogenaemia | Is a | True | Factor I deficiency disease | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR