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 |
| 1773757014 | Familial hypercholesterolaemia due to heterozygous LDL receptor mutation | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 1775043017 | Familial hypercholesterolemia due to heterozygous LDL receptor mutation | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 2972405018 | Familial hypercholesterolemia due to heterozygous low density lipoprotein receptor mutation | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2972595014 | Familial hypercholesterolemia due to heterozygous low density lipoprotein receptor mutation (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3035741011 | Familial hypercholesterolaemia due to heterozygous low density lipoprotein receptor mutation | 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 |
| Familial hypercholesterolaemia due to heterozygous LDL receptor mutation | est un(e) (attribut) | Familial hypercholesterolemia (disorder) | true | Inferred relationship | Some | ||
| Familial hypercholesterolaemia due to heterozygous LDL receptor mutation | localisation d'une constatation (attribut) | structure d'un système corporel | false | Inferred relationship | Some | ||
| Familial hypercholesterolaemia due to heterozygous LDL receptor mutation | est défini par la manifestation de (attribut) | taux de cholestérol sérique augmenté | false | Inferred relationship | Some | ||
| Familial hypercholesterolaemia due to heterozygous LDL receptor mutation | a pour interprétation (attribut) | au-dessus de l'étendue de référence | true | Inferred relationship | Some | 1 | |
| Familial hypercholesterolaemia due to heterozygous LDL receptor mutation | interprète (attribut) | Serum total cholesterol measurement (procedure) | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Canada English language reference set (foundation metadata concept)
Description inactivation indicator reference set
FHIR