Status: current, Defined. Date: 31-Jan 2010. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2836661013 | Clinical finding not suspected (situation) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 2841940017 | Clinical finding not suspected | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Clinical finding not suspected | Is a | Possible clinical finding | false | Inferred relationship | Some | ||
| Clinical finding not suspected | Finding context | NOT suspected | true | Inferred relationship | Some | 1 | |
| Clinical finding not suspected | Subject relationship context | Subject of record | true | Inferred relationship | Some | 3 | |
| Clinical finding not suspected | Temporal context | Current or specified | true | Inferred relationship | Some | 2 | |
| Clinical finding not suspected | Is a | Finding with explicit context | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Congenital hypothyroidism not suspected | Is a | True | Clinical finding not suspected | Inferred relationship | Some | |
| Cystic fibrosis not suspected | Is a | True | Clinical finding not suspected | Inferred relationship | Some | |
| Medium-chain acyl-coenzyme A dehydrogenase deficiency not suspected | Is a | True | Clinical finding not suspected | Inferred relationship | Some | |
| Phenylketonuria not suspected | Is a | True | Clinical finding not suspected | Inferred relationship | Some | |
| Sickle cell trait not suspected | Is a | True | Clinical finding not suspected | Inferred relationship | Some | |
| Sickle cell disease not suspected | Is a | True | Clinical finding not suspected | Inferred relationship | Some | |
| Ebola virus disease not suspected | Is a | True | Clinical finding not suspected | Inferred relationship | Some |
Reference Sets
Situation with explicit context foundation reference set
Problem/Diagnosis reference set
FHIR