Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 332851016 | Central nervous system deficit | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 607047015 | Central nervous system deficit (finding) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 1713591000052112 | bortfallssymtom som rör centrala nervsystemet | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Central nervous system deficit | Is a | Neurological finding | false | Inferred relationship | Some | ||
| Central nervous system deficit | Finding site | Structure of nervous system (body structure) | false | Inferred relationship | Some | ||
| Central nervous system deficit | Interprets | Nervous system function | false | Inferred relationship | Some | ||
| Central nervous system deficit | Is a | Neurological deficit | true | Inferred relationship | Some | ||
| Central nervous system deficit | Is a | Central nervous system finding | true | Inferred relationship | Some | ||
| Central nervous system deficit | Finding site | Structure of central nervous system (body structure) | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| vid undersökning: bortfallssymtom som rör centrala nervsystemet | Associated finding | False | Central nervous system deficit | Inferred relationship | Some | 1 |
| vid undersökning: bortfallssymtom som rör centrala nervsystemet | Is a | False | Central nervous system deficit | Inferred relationship | Some |
This concept is not in any reference sets
FHIR