Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Arteriopathic granular atrophy of cerebral cortex (disorder) |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Cortex laceration |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Disorder of visual cortex |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Corticobasal degeneration |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Progressive sclerosing poliodystrophy |
Is a |
False |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Contusion of cerebral cortex |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Cerebral ataxia |
Is a |
False |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Polioencephalopathy |
Is a |
False |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Cerebral cortical dysgenesis |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Aphasia-angular gyrus syndrome |
Is a |
False |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Cerebral compression due to injury (disorder) |
Is a |
False |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Cortical hemorrhage |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Ectopic gray matter in centrum ovale |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Premotor cortex syndrome |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Rhinocerebral mucormycosis |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Malignant neoplasm of cerebral cortex |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Visual cortex injury |
Is a |
False |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Cortex laceration without mention of open intracranial wound |
Is a |
False |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Cortex laceration and contusion |
Is a |
False |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
dysplasie du cortex cérébral |
Is a |
False |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
A type of focal epilepsy where all the seizures originate within the mesiobasal limbic area of the temporal lobe. |
Is a |
False |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
A type of focal epilepsy where all the seizures originate within the amygdalo-hippocampal area of the temporal lobe. |
Is a |
False |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
A type of focal epilepsy where all the seizures originate within the cingulate area of the frontal lobe. |
Is a |
False |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Uncinate herniation |
Is a |
False |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Cortical visual impairment (disorder) |
Is a |
False |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Visual cortex injury |
Is a |
False |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Macrogyria |
Is a |
False |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Cerebral cortex myoclonus (disorder) |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
A rare neurologic disease characterized by impairment of higher visual processing skills and other posterior cortical functions without any evidence of ocular abnormalities, relatively intact memory and language in the early stages, and atrophy of posterior brain regions. |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
A rare, inherited disorder characterized by widespread calcifications of basal ganglia and cortex, developmental delay, small stature, retinopathy and microcephaly. The absence of progressive deterioration of the neurological functions is characteristic of the disease. |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Progressive focal cortical atrophy |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Cortical dysplasia |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Cortex laceration with open intracranial wound |
Is a |
False |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
A rare, genetic, central nervous system malformation syndrome characterized by congenital, progressive microcephaly, neonatal to infancy-onset of severe, intractable seizures, and diffuse cerebral cortex and cerebellar vermis atrophy with mild cerebellar hemisphere atrophy, associated with profound global developmental delay. Hypotonia or hypertonia with brisk reflexes, variable dysmorphic facial features, ophthalmological signs (cortical visual impairment, nystagmus, eye deviation) and episodes of sudden extreme agitation caused by severe illness may also be associated. |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Sensory somatic cortical disorder |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Microdysgenesis |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Motor cortical disorder |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Speech cortex disorder |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Mesial temporal lobe epilepsy with hippocampal sclerosis is a rare epilepsy syndrome defined by seizures originating in limbic areas of the mesial temporal lobe, particularly in the hippocampus, amygdala, and in the parahippocampal gyrus and its connections, and hippocampal sclerosis, usually unilateral or asymmetric. It is frequently associated with an initial precipitating event, such as febrile seizures, hypoxia, intracranial infection or head trauma, most often occurring in the first five years of life, followed by a latent period without seizures. Typical seizures consist of a characteristic aura that is frequently a rising epigastric sensation associated with emotional disturbances, illusions, and autonomic symptoms (widened pupils, palpitations), progressive impairment of consciousness, oro-alimentary automatisms (lip smacking, chewing, licking, tooth grinding), behavioral arrest, head deviation, dystonic postures, hand and verbal automatisms. Seizures are followed by postictal dysfunction. Initially, seizures are easily controlled with antiepileptic drugs, later they frequently become refractory and associated with progressive behavioral changes and memory deficits. |
Is a |
False |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Cortical vascular dementia (disorder) |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Van Bogaert's sclerosing leukoencephalitis |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Bilateral frontal polymicrogyria |
Is a |
False |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Bilateral frontoparietal polymicrogyria is a sub-type of polymicrogyria. It is a cerebral cortical malformation characterized by excessive cortical folding and abnormal cortical layering, that involves the frontoparietal region of the brain and that presents with hypotonia, developmental delay, moderate to severe intellectual disability, pyramidal signs, epileptic seizures, non progressive cerebellar ataxia, dysconjugate gaze and/or strabismus. |
Is a |
False |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Bilateral generalized polymicrogyria (disorder) |
Is a |
False |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Bilateral parasagittal parieto-occipital polymicrogyria |
Is a |
False |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Progressive supranuclear palsy parkinsonism syndrome (disorder) |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Progressive supranuclear palsy progressive non fluent aphasia |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
A rare, genetic, neurodevelopmental disorder with primordial microcephaly characterized by primary microcephaly, moderate to severe intellectual disability, and global developmental delay. Variable brain malformations are common ranging from simplified gyration, to cortical malformations such as pachygyria, polymicrogyria, reduced sulcation and midline defects. Craniofacial dysmorphism (e.g. sloping forehead, high and broad nasal bridge) are related to the primary microcephaly. Short stature is frequently observed and may be severe. |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
A rare, genetic, complex cerebral cortical malformation characterized by generalized or focal dysgyria (also named polymicrogyria-like cortical dysplasia) or alternatively by microlissencephaly with dysmorphic basal ganglia and dysgenesis of the corpus callosum. Clinical manifestations are variable and include microcephaly, seizures, hypotonia, developmental delay, severe psychomotor delay, ataxia, spastic diplegia or tetraplegia, and ocular abnormalities (strabismus, ptosis or optic atrophy). |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
A rare neurologic disease characterized by multifaceted motor system dysfunctions and cognitive defects such as asymmetric rigidity, bradykinesia, limb apraxia, and visuospatial dysfunction. |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
A type of focal epilepsy where all the seizures originate within the opercular area of the frontal lobe. |
Is a |
False |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
A type of focal epilepsy where all the seizures originate within the primary motor cortex area of the frontal lobe. |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
A type of focal epilepsy where all the seizures originate within the anterior frontopolar area of the frontal lobe. |
Is a |
False |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Infantile Convulsions and paroxysmal ChoreoAthetosis (ICCA) syndrome is a neurological condition characterised by the occurrence of seizures during the first year of life and choreoathetotic dyskinetic attacks during childhood or adolescence. |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Atrophy of cortex of occipital lobe (disorder) |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Atrophy of cortex of parietal lobe |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Atrophy of cortex of temporal lobe |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Atrophy of cortex of frontal lobe (disorder) |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Atrophy of hippocampus |
Is a |
False |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Frontotemporal dementia with parkinsonism-17 |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Congenital dysplasia of fronto-parietal cortex (disorder) |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|
Hemiatrophy of cerebral cortex |
Is a |
True |
Disorder of cerebral cortex |
Inferred relationship |
Some |
|