Status: current, Primitive. Date: 31-Jul 2003. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1770709016 | Primary genetic hyperlipidemia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 1773669014 | Primary genetic hyperlipidaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 1774955016 | Primary genetic hyperlipidemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Primary genetic hyperlipidaemia | Is a | Endogenous hyperlipidaemia | true | Inferred relationship | Some | ||
| Primary genetic hyperlipidaemia | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Primary genetic hyperlipidaemia | Has definitional manifestation | Serum lipids high | false | Inferred relationship | Some | ||
| Primary genetic hyperlipidaemia | Has definitional manifestation | Lipid above reference range | false | Inferred relationship | Some | ||
| Primary genetic hyperlipidaemia | Interprets | Lipids measurement | true | Inferred relationship | Some | 1 | |
| Primary genetic hyperlipidaemia | Has interpretation | Above reference range | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Chylomicronemia syndrome | Is a | True | Primary genetic hyperlipidaemia | Inferred relationship | Some | |
| Primary genetic mixed hyperlipidaemia | Is a | True | Primary genetic hyperlipidaemia | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR