Status: current, Primitive. Date: 31-Jan 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4168312019 | Focal cortical dysplasia type Ia | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
4168313012 | Focal cortical dysplasia type Ia (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
4168598017 | Focal cortical dysplasia is a congenital abnormality with abnormal organisation of the cortical layers of the brain. These lesions frequently cause refractory epilepsy. Type Ia presents late with mild symptoms and is more often seen in adults. Changes are present in the temporal lobe and are restricted to cortical dyslamination. | en | Definition | Active | Case sensitive | SNOMED CT core |
4168599013 | Focal cortical dysplasia is a congenital abnormality with abnormal organization of the cortical layers of the brain. These lesions frequently cause refractory epilepsy. Type Ia presents late with mild symptoms and is more often seen in adults. Changes are present in the temporal lobe and are restricted to cortical dyslamination. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Focal cortical dysplasia type Ia | Is a | Localised cortical dysplasia | true | Inferred relationship | Some | ||
Focal cortical dysplasia type Ia | Associated morphology | Dysplasia | true | Inferred relationship | Some | 1 | |
Focal cortical dysplasia type Ia | Finding site | Structure of cerebral cortex | true | Inferred relationship | Some | 1 | |
Focal cortical dysplasia type Ia | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Focal cortical dysplasia type Ia | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set