Status: current, Defined. Date: 28-Feb 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2788736011 | Hereditary antithrombin III deficiency (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
2791100010 | Hereditary antithrombin III deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hereditary antithrombin III deficiency | Interprets | Haemostatic function | true | Inferred relationship | Some | 1 | |
Hereditary antithrombin III deficiency | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 | |
Hereditary antithrombin III deficiency | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Hereditary antithrombin III deficiency | Interprets | Measurement of antithrombin III activity in plasma | true | Inferred relationship | Some | 2 | |
Hereditary antithrombin III deficiency | Has interpretation | Abnormally low | true | Inferred relationship | Some | 2 | |
Hereditary antithrombin III deficiency | Is a | Hereditary thrombophilia | true | Inferred relationship | Some | ||
Hereditary antithrombin III deficiency | Is a | Antithrombin III deficiency | true | 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