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 |
4168225012 | Focal cortical dysplasia type IIa | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
4168226013 | Focal cortical dysplasia type IIa (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
4166792010 | Focal cortical dysplasia is a congenital abnormality with abnormal organisation of the cortical layers of the brain. These lesions frequently cause refractory epilepsy. Type II usually presents in children. More extensive changes occur outside the temporal lobe and commonly in the frontal lobe. Type IIa is histologically distinct due to the absence of balloon cells. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
4166793017 | Focal cortical dysplasia is a congenital abnormality with abnormal organization of the cortical layers of the brain. These lesions frequently cause refractory epilepsy. Type II usually presents in children. More extensive changes occur outside the temporal lobe and commonly in the frontal lobe. Type IIa is histologically distinct due to the absence of balloon cells. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
4168225012 | Focal cortical dysplasia type IIa | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
4168226013 | Focal cortical dysplasia type IIa (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
4166792010 | Focal cortical dysplasia is a congenital abnormality with abnormal organisation of the cortical layers of the brain. These lesions frequently cause refractory epilepsy. Type II usually presents in children. More extensive changes occur outside the temporal lobe and commonly in the frontal lobe. Type IIa is histologically distinct due to the absence of balloon cells. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
4166793017 | Focal cortical dysplasia is a congenital abnormality with abnormal organization of the cortical layers of the brain. These lesions frequently cause refractory epilepsy. Type II usually presents in children. More extensive changes occur outside the temporal lobe and commonly in the frontal lobe. Type IIa is histologically distinct due to the absence of balloon cells. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
6168931000241116 | dysplasie corticale focale de type IIa | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6168931000241116 | dysplasie corticale focale de type IIa | 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 IIa | Is a | Localised cortical dysplasia | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
Focal cortical dysplasia type IIa | Associated morphology | Dysplasia | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 | |
Focal cortical dysplasia type IIa | Finding site | Cerebral cortex | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 | |
Focal cortical dysplasia type IIa | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 | |
Focal cortical dysplasia type IIa | 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