Status: current, Not sufficiently defined by necessary conditions definition status. Date: 28-Sep 2022. Module: SNOMED CT United Kingdom Edition module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 307611000237111 | Genetic variant causing familial hypercholesterolaemia not detected | en | Synonym | Active | Entire term case insensitive | SNOMED CT United Kingdom Edition module |
| 307621000237119 | Genetic variant causing familial hypercholesterolaemia not detected (finding) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT United Kingdom Edition module |
| 307631000237117 | Genetic variant causing FH (familial hypercholesterolaemia) not detected | en | Synonym | Active | Only initial character case insensitive | SNOMED CT United Kingdom Edition module |
| 307641000237112 | Genetic variant causing familial hypercholesterolaemia detection result negative | en | Synonym | Active | Entire term case insensitive | SNOMED CT United Kingdom Edition module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Genetic variant causing familial hypercholesterolaemia not detected | Is a | Clinical finding | true | Inferred relationship | Existential restriction modifier | ||
| Genetic variant causing familial hypercholesterolaemia not detected | Interprets | Familial hypercholesterolaemia comprehensive genetic test result | true | Inferred relationship | Existential restriction modifier | 1 | |
| Genetic variant causing familial hypercholesterolaemia not detected | Has interpretation | Not detected | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR