Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 398860018 | Hyperchylomicronemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 398861019 | Primary hyperchylomicronemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 398862014 | Primary hyperchylomicronaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 398863016 | Familial hyperchylomicronemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 398865011 | Burger-Grutz syndrome | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 398867015 | Familial hyperchylomicronaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 398868013 | Hyperchylomicronaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 660051013 | Familial hyperchylomicronemia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial hyperchylomicronaemia | Is a | Familial hypertriglyceridaemia | true | Inferred relationship | Some | ||
| Familial hyperchylomicronaemia | Has definitional manifestation | Serum lipids high | false | Inferred relationship | Some | ||
| Familial hyperchylomicronaemia | Has definitional manifestation | Lipid above reference range | false | Inferred relationship | Some | ||
| Familial hyperchylomicronaemia | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Familial hyperchylomicronaemia | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Familial hyperchylomicronaemia | Is a | Primary hypertriglyceridaemia | false | Inferred relationship | Some | ||
| Familial hyperchylomicronaemia | Interprets | Lipids measurement | true | Inferred relationship | Some | 1 | |
| Familial hyperchylomicronaemia | Has interpretation | Above reference range | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Familial apolipoprotein C-II deficiency | Is a | False | Familial hyperchylomicronaemia | Inferred relationship | Some | |
| Familial lipoprotein lipase deficiency with type I phenotype | Is a | True | Familial hyperchylomicronaemia | Inferred relationship | Some | |
| Familial lipoprotein lipase deficiency with type V phenotype | Is a | True | Familial hyperchylomicronaemia | Inferred relationship | Some |
Reference Sets
Emergency department reference set
Australian emergency department reference set
NSW Emergency Department reference set
Clinical finding foundation reference set
Emergency department diagnosis reference set
Problem/Diagnosis reference set
FHIR