Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4168308013 | Focal cortical dysplasia type Ib | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
4168309017 | Focal cortical dysplasia type Ib (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
4168308013 | Focal cortical dysplasia type Ib | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
4168309017 | Focal cortical dysplasia type Ib (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
4168602015 | 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 include cortical dyslamination and giant or immature neurones. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
4168603013 | 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 include cortical dyslamination and giant or immature neurones. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
6218401000241117 | dysplasie corticale focale de type Ib | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6218401000241117 | dysplasie corticale focale de type Ib | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Focal cortical dysplasia type Ib | Is a | Localised cortical dysplasia | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
Focal cortical dysplasia type Ib | Associated morphology | Dysplasia | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 | |
Focal cortical dysplasia type Ib | Finding site | Cerebral cortex | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 | |
Focal cortical dysplasia type Ib | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 | |
Focal cortical dysplasia type Ib | Pathological process (attribute) | Pathological developmental process (qualifier value) | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets