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 |
| 1771753018 | Familial lipoprotein lipase deficiency with type I phenotype (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 1782834011 | Familial lipoprotein lipase deficiency with type I phenotype | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 1783801016 | Familial type I hyperlipoproteinaemia | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 1784187010 | Familial type I hyperlipoproteinemia | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial lipoprotein lipase deficiency with type I phenotype (disorder) | est un(e) (attribut) | Familial hyperchylomicronemia | true | Inferred relationship | Some | ||
| Familial lipoprotein lipase deficiency with type I phenotype (disorder) | localisation d'une constatation (attribut) | structure d'un système corporel | false | Inferred relationship | Some | ||
| Familial lipoprotein lipase deficiency with type I phenotype (disorder) | est défini par la manifestation de (attribut) | Serum lipids high | false | Inferred relationship | Some | ||
| Familial lipoprotein lipase deficiency with type I phenotype (disorder) | est défini par la manifestation de (attribut) | Increased lipid | false | Inferred relationship | Some | ||
| Familial lipoprotein lipase deficiency with type I phenotype (disorder) | interprète (attribut) | Lipids measurement | true | Inferred relationship | Some | 1 | |
| Familial lipoprotein lipase deficiency with type I phenotype (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 |
This concept is not in any reference sets
FHIR