Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3309285015 | Congenital plasminogen activator inhibitor deficiency type 1 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3309286019 | Congenital plasminogen activator inhibitor deficiency type 1 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5401575017 | A rare hemorrhagic disorder due to a constitutional hemostatic factors defect characterized by premature lysis of hemostatic clots and a moderate bleeding tendency. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401576016 | A rare haemorrhagic disorder due to a constitutional haemostatic factors defect characterised by premature lysis of haemostatic clots and a moderate bleeding tendency. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital plasminogen activator inhibitor deficiency type 1 (disorder) | Is a | Hereditary coagulation factor deficiency | true | Inferred relationship | Some | ||
Congenital plasminogen activator inhibitor deficiency type 1 (disorder) | Is a | Congenital disease (disorder) | true | Inferred relationship | Some | ||
Congenital plasminogen activator inhibitor deficiency type 1 (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Congenital plasminogen activator inhibitor deficiency type 1 (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Congenital plasminogen activator inhibitor deficiency type 1 (disorder) | Has interpretation | Abnormal | true | Inferred relationship | Some | 2 | |
Congenital plasminogen activator inhibitor deficiency type 1 (disorder) | Interprets | Hemostatic function | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)