Status: current, Primitive. Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3758307019 | Familial thrombomodulin anomalies (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 3758308012 | Familial thrombomodulin anomalies | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3758309016 | A rare life-threatening genetic coagulation disorder with characteristics of an increased risk of blood clot formation in several members of a family due to a thrombomodulin gene mutation. Patients may manifest with venous thromboembolic disease, premature myocardial infarction and/or arterial thrombosis. | en | Definition | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial thrombomodulin anomalies | Is a | Familial disease | true | Inferred relationship | Some | ||
| Familial thrombomodulin anomalies | Is a | Blood coagulation disorder | true | Inferred relationship | Some | ||
| Familial thrombomodulin anomalies | Interprets | Haemostatic function | true | Inferred relationship | Some | 1 | |
| Familial thrombomodulin anomalies | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR