Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
chorée de Bergeron |
Is a |
False |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Dystonia |
Is a |
True |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Chronic progressive non-hereditary chorea |
Is a |
False |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Progressive cerebellar tremor |
Is a |
True |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Athetosis (disorder) |
Is a |
True |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Birnbaum's syndrome (disorder) |
Is a |
False |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Orofacial dyskinesia |
Is a |
True |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Gilles de la Tourette's syndrome |
Is a |
True |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Paramyoclonus multiplex |
Is a |
True |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Electric chorea (disorder) |
Is a |
True |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Abortive cerebellar ataxia |
Is a |
False |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Familial essential myoclonus (disorder) |
Is a |
True |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Olivopontocerebellar degeneration |
Is a |
True |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Dentatorubropallidoluysian degeneration |
Is a |
False |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Disorder of basal ganglia (disorder) |
Is a |
False |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Dyssynergia cerebellaris myoclonica (disorder) |
Is a |
True |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
A form of dyskinetic cerebral palsy with slow, writhing movements that are often repetitive, sinuous, and rhythmic. |
Is a |
False |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Combined pyramidal-extrapyramidal syndrome (disorder) |
Is a |
True |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Juvenile cerebellar degeneration AND myoclonus |
Is a |
True |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Opticocochleodentate degeneration |
Is a |
True |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Diffuse Lewy body disease (disorder) |
Is a |
True |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Henoch's chorea |
Is a |
False |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Progressive pyramidopallidal degeneration |
Is a |
True |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hemichorea |
Is a |
False |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Neuroleptic malignant syndrome |
Is a |
True |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
syndrome de Shy-Drager |
Is a |
False |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Corticobasal degeneration |
Is a |
True |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Pallidoluysian degeneration |
Is a |
False |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Pigmentary pallidal degeneration |
Is a |
False |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Parkinsonism |
Is a |
True |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Pallidopontonigral degeneration |
Is a |
False |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Choreoathetosis |
Is a |
False |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Juvenile paralysis agitans of Hunt (disorder) |
Is a |
False |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Huntington's chorea |
Is a |
False |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Pallidonigroluysian degeneration |
Is a |
True |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hemiballism |
Is a |
True |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Choreoacanthocytosis |
Is a |
False |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Pallidonigral degeneration |
Is a |
False |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Pallidonigrospinal degeneration |
Is a |
False |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
A less common type of cerebral palsy defined by decreased and/or fluctuating muscle tone; multiple forms of non-spastic cerebral palsy are each characterised by particular impairments; one of the main characteristics of non-spastic cerebral palsy is involuntary movement. Subtypes include ataxic and dyskinetic forms. |
Is a |
True |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Huntington disease-like syndrome |
Is a |
False |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
A rare severe neurodegenerative disorder that is considered one of the phenocopies of Huntington Disease (HD) affecting patients of African descent and characterized by a triad of movement (chorea, oculomotor, parkinsonism), psychiatric (prominently sadness, irritability and anxiety), and cognitive abnormalities (early cognitive decline and subcortical-like dementia). |
Is a |
False |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
McLeod neuroacanthocytosis syndrome (disorder) |
Is a |
True |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Myoclonus, cerebellar ataxia, deafness syndrome |
Is a |
True |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Proximal myopathy with extrapyramidal signs |
Is a |
True |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Woodhouse Sakati syndrome |
Is a |
True |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder) |
Is a |
False |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
A very rare genetic disorder characterized by the following congenital malformations: hydrocephalus (due to Dandy-Walker anomaly), cleft palate, and severe joint contractures. |
Is a |
True |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Benedikt's syndrome |
Is a |
True |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder |
Is a |
True |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Progressive supranuclear ophthalmoplegia (disorder) |
Is a |
True |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
A rare, syndromic intellectual disability characterized by macrocephaly, short stature, intellectual disability, variable degree of spastic paraplegia, central nervous system malformations (hydrocephalus, Dandy-Walker malformation), and dysmorphic features, such as high and broad forehead, midface hypoplasia, and small and broad hands and feet. There have been no further descriptions in the literature since 1993. |
Is a |
True |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Chorea (disorder) |
Is a |
True |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital pontocerebellar hypoplasia type 12 |
Is a |
True |
Extrapyramidal disease |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|