Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 351266019 | Congenital factor IX deficiency variant | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 622763015 | Congenital factor IX deficiency variant (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital factor IX deficiency variant | Has interpretation | Abnormal | true | Inferred relationship | Some | 2 | |
| Congenital factor IX deficiency variant | Interprets | Haemostatic function | true | Inferred relationship | Some | 2 | |
| Congenital factor IX deficiency variant | Is a | Congenital disease | false | Inferred relationship | Some | ||
| Congenital factor IX deficiency variant | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Congenital factor IX deficiency variant | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Congenital factor IX deficiency variant | Has definitional manifestation | Haemostatic system finding | false | Inferred relationship | Some | ||
| Congenital factor IX deficiency variant | Is a | Hereditary factor IX deficiency disease | true | Inferred relationship | Some | ||
| Congenital factor IX deficiency variant | 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
Australian dialect reference set
Problem/Diagnosis reference set
FHIR