Status: current, Primitive. Date: 31-Jan 2009. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2790009017 | Congenital dysmegakaryopoietic thrombocytopenia, Paris Trousseau type (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
2791002017 | Congenital dysmegakaryopoietic thrombocytopenia, Paris Trousseau type | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital dysmegakaryopoietic thrombocytopenia, Paris Trousseau type | Interprets | Haemostatic function | false | Inferred relationship | Some | 2 | |
Congenital dysmegakaryopoietic thrombocytopenia, Paris Trousseau type | Has interpretation | Abnormal | true | Inferred relationship | Some | 2 | |
Congenital dysmegakaryopoietic thrombocytopenia, Paris Trousseau type | Interprets | Haemostatic function | true | Inferred relationship | Some | 2 | |
Congenital dysmegakaryopoietic thrombocytopenia, Paris Trousseau type | Is a | Hereditary thrombocytopenic disorder | true | Inferred relationship | Some | ||
Congenital dysmegakaryopoietic thrombocytopenia, Paris Trousseau type | Has definitional manifestation | Platelet count below reference range | false | Inferred relationship | Some | ||
Congenital dysmegakaryopoietic thrombocytopenia, Paris Trousseau type | Finding site | Body system structure | true | Inferred relationship | Some | 3 | |
Congenital dysmegakaryopoietic thrombocytopenia, Paris Trousseau type | Has interpretation | Below reference range | true | Inferred relationship | Some | 1 | |
Congenital dysmegakaryopoietic thrombocytopenia, Paris Trousseau type | Interprets | Platelet count | 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