Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3674045015 | Factor IX deficiency (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
| 3674046019 | Factor IX deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Factor IX deficiency | Interprets | Haemostatic function | true | Inferred relationship | Some | 1 | |
| Factor IX deficiency | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 | |
| Factor IX deficiency | Is a | Coagulation factor deficiency syndrome | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Hereditary factor IX deficiency disease | Is a | True | Factor IX deficiency | Inferred relationship | Some | |
| Acquired factor IX deficiency disease | Is a | True | Factor IX deficiency | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR