Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 139364010 | Familial multiple factor deficiency syndrome, type I | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 139365011 | FMFD syndrome, type I | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 139366012 | Factor V and factor VIII deficiency | en | Synonym | Inactive | Initial character case insensitive | SNOMED CT core |
| 139367015 | Factor V AND factor VIII deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 825809015 | Familial multiple factor deficiency syndrome, type I (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial multiple factor deficiency syndrome, type I | Interprets | Haemostatic function | true | Inferred relationship | Some | 1 | |
| Familial multiple factor deficiency syndrome, type I | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 | |
| Familial multiple factor deficiency syndrome, type I | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Familial multiple factor deficiency syndrome, type I | Has definitional manifestation | Haemostatic system finding | false | Inferred relationship | Some | ||
| Familial multiple factor deficiency syndrome, type I | Is a | Familial multiple factor deficiency syndrome | true | Inferred relationship | Some | ||
| Familial multiple factor deficiency syndrome, type I | 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
Problem/Diagnosis reference set