Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 158737014 | Hereditary hypoplasminogenemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 512324012 | Hereditary hypoplasminogenaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 840080012 | Hereditary hypoplasminogenemia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary hypoplasminogenaemia | Interprets | Haemostatic function | true | Inferred relationship | Some | 1 | |
| Hereditary hypoplasminogenaemia | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 | |
| Hereditary hypoplasminogenaemia | Is a | Hereditary disorder by system | false | Inferred relationship | Some | ||
| Hereditary hypoplasminogenaemia | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Hereditary hypoplasminogenaemia | Has definitional manifestation | Haemostatic system finding | false | Inferred relationship | Some | ||
| Hereditary hypoplasminogenaemia | Is a | Hypoplasminogenaemia | true | Inferred relationship | Some | ||
| Hereditary hypoplasminogenaemia | Is a | Hereditary disorder of haematologic system | false | Inferred relationship | Some | ||
| Hereditary hypoplasminogenaemia | Is a | Hereditary disease | true | Inferred relationship | Some | ||
| Hereditary hypoplasminogenaemia | Finding site | Entire haematological system | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Autosomal dominant deficiency of plasminogen | Is a | True | Hereditary hypoplasminogenaemia | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR