Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 158735018 | Hypoplasminogenemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 512322011 | Plasminogen deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 512323018 | Hypoplasminogenaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 840078018 | Hypoplasminogenemia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hypoplasminogenaemia | Interprets | Haemostatic function | true | Inferred relationship | Some | 1 | |
| Hypoplasminogenaemia | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 | |
| Hypoplasminogenaemia | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Hypoplasminogenaemia | Has definitional manifestation | Haemostatic system finding | false | Inferred relationship | Some | ||
| Hypoplasminogenaemia | Is a | Fibrinolytic bleeding syndrome | true | Inferred relationship | Some | ||
| Hypoplasminogenaemia | Is a | Disorder involving the fibrinolytic system | false | Inferred relationship | Some | ||
| Hypoplasminogenaemia | Finding site | Entire haematological system | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Hereditary hypoplasminogenaemia | Is a | True | Hypoplasminogenaemia | Inferred relationship | Some | |
| Acquired hypoplasminogenaemia | Is a | True | Hypoplasminogenaemia | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR