Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2003. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1771757017 | Familial hypercholesterolemia due to genetic defect of apolipoprotein B (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| 1773759012 | Familial hypercholesterolaemia due to genetic defect of apolipoprotein B | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 1775045012 | Familial hypercholesterolemia due to genetic defect of apolipoprotein B | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 1783802011 | Familial Combined Hypercholesterolaemia | en | Synonym | Inactive | Only initial character case insensitive | SNOMED CT core module |
| 1783803018 | Hypercholesterolaemia due to apolipoprotein B gene defect | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 1784188017 | Hypercholesterolemia due to apolipoprotein B gene defect | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 1784189013 | Familial Combined Hypercholesterolemia | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial hypercholesterolemia due to genetic defect of apolipoprotein B | Is a | Familial hypercholesterolemia | true | Inferred relationship | Existential restriction modifier | ||
| Familial hypercholesterolemia due to genetic defect of apolipoprotein B | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier | ||
| Familial hypercholesterolemia due to genetic defect of apolipoprotein B | Has definitional manifestation | Serum cholesterol above reference range | false | Inferred relationship | Existential restriction modifier | ||
| Familial hypercholesterolemia due to genetic defect of apolipoprotein B | Has interpretation | Above reference range | true | Inferred relationship | Existential restriction modifier | 1 | |
| Familial hypercholesterolemia due to genetic defect of apolipoprotein B | Interprets | Serum total cholesterol measurement | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Familial hypercholesterolaemia due to genetic defect of apolipoprotein B-100 | Is a | False | Familial hypercholesterolemia due to genetic defect of apolipoprotein B | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR