Status: current, Primitive. Date: 31-Jul 2003. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1770710014 | Chylomicronemia syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 1781879012 | Chylomicronemia syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Chylomicronemia syndrome | Is a | Primary chylomicronemia | true | Inferred relationship | Some | ||
| Chylomicronemia syndrome | Is a | Primary genetic hyperlipidaemia | true | Inferred relationship | Some | ||
| Chylomicronemia syndrome | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Chylomicronemia syndrome | Has definitional manifestation | Serum lipids high | false | Inferred relationship | Some | ||
| Chylomicronemia syndrome | Has definitional manifestation | Lipid above reference range | false | Inferred relationship | Some | ||
| Chylomicronemia syndrome | Has interpretation | Above reference range | true | Inferred relationship | Some | 1 | |
| Chylomicronemia syndrome | Interprets | Lipids measurement | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Familial chylomicronemia syndrome | Is a | True | Chylomicronemia syndrome | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR