Status: current, Primitive. Date: 28-Feb 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4697310014 | THBD (thrombomodulin) related bleeding disorder | en | Synonym | Active | Case sensitive | SNOMED CT core |
4697311013 | Thrombomodulin-related bleeding disorder (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
4697312018 | Thrombomodulin-related bleeding disorder | en | Synonym | Active | Case insensitive | SNOMED CT core |
4697313011 | Thrombomodulin-related coagulopathy | en | Synonym | Active | Case insensitive | SNOMED CT core |
4697318019 | A rare genetic coagulation disorder characterised by marked bleeding tendency and posttraumatic bleeding with easy bruising, soft tissue and muscle bleeding, haemarthroses and menorrhagia. Caused by an increase of soluble thrombomodulin in plasma with subsequent protein C activation and reduction of thrombin generation within a potential thrombus. Abnormal laboratory findings include markedly elevated plasma thrombomodulin, reduced prothrombin consumption and decreased thrombin generation. | en | Definition | Active | Case sensitive | SNOMED CT core |
4697319010 | A rare genetic coagulation disorder characterized by marked bleeding tendency and posttraumatic bleeding with easy bruising, soft tissue and muscle bleeding, hemarthroses and menorrhagia. Caused by an increase of soluble thrombomodulin in plasma with subsequent protein C activation and reduction of thrombin generation within a potential thrombus. Abnormal laboratory findings include markedly elevated plasma thrombomodulin, reduced prothrombin consumption and decreased thrombin generation. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Thrombomodulin-related bleeding disorder | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Thrombomodulin-related bleeding disorder | Is a | Blood coagulation disorder | true | Inferred relationship | Some | ||
Thrombomodulin-related bleeding disorder | Interprets | Haemostatic function | true | Inferred relationship | Some | 1 | |
Thrombomodulin-related bleeding disorder | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set