Status: current, Primitive. Date: 31-Jul 2004. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2468183016 | Negative genetic finding (finding) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 2474288014 | Negative genetic finding | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| BRCA1 gene mutation negative | Is a | False | Negative genetic finding | Inferred relationship | Some | |
| BRCA2 gene mutation negative | Is a | False | Negative genetic finding | Inferred relationship | Some | |
| Breast cancer genetic marker of susceptibility negative | Is a | True | Negative genetic finding | Inferred relationship | Some | |
| Mitochondrial 1555 A to G mutation negative | Is a | True | Negative genetic finding | Inferred relationship | Some | |
| Human epidermal growth factor 2 gene amplification negative | Is a | True | Negative genetic finding | Inferred relationship | Some | |
| HLA-B*57:01 negative | Is a | True | Negative genetic finding | Inferred relationship | Some | |
| HLA-A*31:01 negative | Is a | True | Negative genetic finding | Inferred relationship | Some | |
| HLA-B*15:02 negative | Is a | True | Negative genetic finding | Inferred relationship | Some | |
| HLA-B*58:01 negative | Is a | True | Negative genetic finding | Inferred relationship | Some |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR