Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Localised cortical dysplasia |
Finding site |
True |
Cerebral cortex |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Isolated focal cortical dysplasia is a rare, genetic, non-syndromic cerebral malformation due to abnormal neuronal migration disorder characterized by variable-sized, focalized malformations located in any part(s) of the cerebral cortex, which manifests with drug-resistant epilepsy (usually leading to intellectual disability) and behavioral disturbances. Abnormal MRI findings (e.g. abnormal white and/or grey matter signal, blurred gray-white matter junction, localized volume loss, cortical thickening, abnormal gyral pattern, abnormal hippocampus) and variable histopathologic patterns are associated. |
Finding site |
True |
Cerebral cortex |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Kortikale Dysplasie-fokale Epilepsie-Syndrom |
Finding site |
False |
Cerebral cortex |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Brain calcification Rajab type (disorder) |
Finding site |
True |
Cerebral cortex |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome (disorder) |
Finding site |
True |
Cerebral cortex |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation |
Finding site |
True |
Cerebral cortex |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Rhinocerebral mucormycosis |
Finding site |
True |
Cerebral cortex |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Sensory somatic cortical disorder |
Finding site |
True |
Cerebral cortex |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Corticobasal degeneration |
Finding site |
True |
Cerebral cortex |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Microdysgenesis |
Finding site |
True |
Cerebral cortex |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Speech cortex disorder (disorder) |
Finding site |
True |
Cerebral cortex |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Cortical vascular dementia |
Finding site |
True |
Cerebral cortex |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Van Bogaert's sclerosing leukoencephalitis |
Finding site |
True |
Cerebral cortex |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Cortex contusion with open intracranial wound AND concussion |
Finding site |
True |
Cerebral cortex |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Cerebral cortex laceration with concussion (disorder) |
Finding site |
True |
Cerebral cortex |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Focal cortical dysplasia type II |
Finding site |
True |
Cerebral cortex |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Focal cortical dysplasia type Ib |
Finding site |
True |
Cerebral cortex |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Focal cortical dysplasia type Ia |
Finding site |
True |
Cerebral cortex |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Focal cortical dysplasia type IIa |
Finding site |
True |
Cerebral cortex |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Focal cortical dysplasia type IIb |
Finding site |
True |
Cerebral cortex |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Progressive supranuclear palsy parkinsonism syndrome (disorder) |
Finding site |
True |
Cerebral cortex |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Progressive supranuclear palsy progressive non fluent aphasia |
Finding site |
True |
Cerebral cortex |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Microcephalic cortical malformations, short stature due to rotatin deficiency (disorder) |
Finding site |
True |
Cerebral cortex |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Polymicrogyria due to TUBB2B mutation |
Finding site |
True |
Cerebral cortex |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Corticobasal syndrome (disorder) |
Finding site |
True |
Cerebral cortex |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Infantile convulsion and choreoathetosis syndrome (disorder) |
Finding site |
True |
Cerebral cortex |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |