Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 1773669014 | Primary genetic hyperlipidaemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 1774955016 | Primary genetic hyperlipidemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Primary genetic hyperlipidemia (disorder) | est un(e) (attribut) | Endogenous hyperlipidaemia | true | Inferred relationship | Some | ||
| Primary genetic hyperlipidemia (disorder) | localisation d'une constatation (attribut) | structure d'un système corporel | false | Inferred relationship | Some | ||
| Primary genetic hyperlipidemia (disorder) | est défini par la manifestation de (attribut) | Serum lipids high | false | Inferred relationship | Some | ||
| Primary genetic hyperlipidemia (disorder) | est défini par la manifestation de (attribut) | Increased lipid | false | Inferred relationship | Some | ||
| Primary genetic hyperlipidemia (disorder) | interprète (attribut) | Lipids measurement | true | Inferred relationship | Some | 1 | |
| Primary genetic hyperlipidemia (disorder) | a pour interprétation (attribut) | au-dessus de l'étendue de référence | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Chylomicronemia syndrome (disorder) | est un(e) (attribut) | True | Primary genetic hyperlipidemia (disorder) | Inferred relationship | Some | |
| Primary genetic mixed hyperlipidemia (disorder) | est un(e) (attribut) | True | Primary genetic hyperlipidemia (disorder) | Inferred relationship | Some |
This concept is not in any reference sets
FHIR