Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Secondary parkinsonism |
Is a |
True |
Parkinsonism |
Inferred relationship |
Some |
|
Multiple system atrophy |
Is a |
False |
Parkinsonism |
Inferred relationship |
Some |
|
Symptomatic parkinsonism |
Is a |
True |
Parkinsonism |
Inferred relationship |
Some |
|
Progressive supranuclear ophthalmoplegia |
Is a |
False |
Parkinsonism |
Inferred relationship |
Some |
|
Striatonigral degeneration |
Is a |
True |
Parkinsonism |
Inferred relationship |
Some |
|
Parkinson's disease |
Is a |
True |
Parkinsonism |
Inferred relationship |
Some |
|
Parkinson-dementia complex of Guam |
Is a |
False |
Parkinsonism |
Inferred relationship |
Some |
|
Parkinsonian syndrome with idiopathic orthostatic hypotension (disorder) |
Is a |
True |
Parkinsonism |
Inferred relationship |
Some |
|
Parkinson's disease NOS |
Is a |
False |
Parkinsonism |
Inferred relationship |
Some |
|
FH: Parkinsonism |
Associated finding |
False |
Parkinsonism |
Inferred relationship |
Some |
1 |
On - off phenomenon (disorder) |
Is a |
False |
Parkinsonism |
Inferred relationship |
Some |
|
Cerebral degeneration due to Parkinson's disease (disorder) |
Due to |
True |
Parkinsonism |
Inferred relationship |
Some |
2 |
FH: Parkinsonism |
Associated finding |
True |
Parkinsonism |
Inferred relationship |
Some |
1 |
FH: Parkinsonism |
Associated finding |
False |
Parkinsonism |
Inferred relationship |
Some |
1 |
X-linked dystonia parkinsonism |
Is a |
True |
Parkinsonism |
Inferred relationship |
Some |
|
Perry syndrome |
Is a |
True |
Parkinsonism |
Inferred relationship |
Some |
|
Abrupt onset of dystonia with parkinsonism over a period of hours to days. |
Is a |
True |
Parkinsonism |
Inferred relationship |
Some |
|
Parkinsonism with dementia of Guadeloupe is characterized by symmetrical bradykinesia, predominantly axial rigidity, postural instability with early falls and cognitive decline with prominent features of frontal lobe dysfunction. |
Is a |
True |
Parkinsonism |
Inferred relationship |
Some |
|
Psychosis co-occurrent and due to Parkinson's disease (disorder) |
Is a |
False |
Parkinsonism |
Inferred relationship |
Some |
|
A rare neurodegenerative disease usually presenting before the age of 30 and which is characterized by dystonia, L-dopa-responsive parkinsonism, pyramidal signs and rapid cognitive decline. |
Is a |
True |
Parkinsonism |
Inferred relationship |
Some |
|
Infantile dystonia-parkinsonism (IPD) is an extremely rare inherited neurological syndrome that presents in early infancy with hypokinetic parkinsonism and dystonia and that can be fatal. |
Is a |
True |
Parkinsonism |
Inferred relationship |
Some |
|
Atypical Parkinsonism (disorder) |
Is a |
True |
Parkinsonism |
Inferred relationship |
Some |
|
Kufor-Rakeb syndrome (KRS) is a rare genetic neurodegenerative disorder characterized by juvenile parkinsonism, pyramidal degeneration (dystonia), supranuclear palsy, and cognitive impairment. |
Is a |
True |
Parkinsonism |
Inferred relationship |
Some |
|
An adult-onset movement disorder characterized by bradykinesia, dysarthria and muscle rigidity. |
Is a |
True |
Parkinsonism |
Inferred relationship |
Some |
|
Infection causing parkinsonism (disorder) |
Is a |
False |
Parkinsonism |
Inferred relationship |
Some |
|
Parkinsonism due to mass lesion of brain (disorder) |
Is a |
True |
Parkinsonism |
Inferred relationship |
Some |
|
Functional parkinsonism (disorder) |
Is a |
True |
Parkinsonism |
Inferred relationship |
Some |
|
Hemiparkinsonism-hemiatrophy syndrome is a rare parkinsonian disorder characterized by unilateral body atrophy and slowly progressive, ipsilateral, hemiparkinsonian signs (bradykinesia, rigidity, and tremor). Patients typically present with unilateral, action-induced dystonia, in upper or lower limbs, that progresses and becomes bilateral or with tremor which occurs predominantly at rest and progresses to hemiparkinsonism. Scoliosis, scapular winging, raised shoulders, brisk reflexes and extensor plantar responses are frequently associated. |
Is a |
True |
Parkinsonism |
Inferred relationship |
Some |
|
A rare, genetic, neurological disorder characterized by parkinsonian features (including resting or action tremor, cogwheel rigidity, hypomimia and bradykinesia) associated with variably penetrant spasticity, hyperactive deep tendon reflexes and Babinski sign. |
Is a |
True |
Parkinsonism |
Inferred relationship |
Some |
|
Dissociative neurological symptom disorder co-occurrent with parkinsonism (disorder) |
Is a |
True |
Parkinsonism |
Inferred relationship |
Some |
|
A rare neuronal ceroid lipofuscinosis disorder characterized by juvenile-onset of progressive spinocerebellar ataxia, bulbar syndrome (manifesting with dysarthria, dysphagia and dysphonia), pyramidal and extrapyramidal involvement (including myoclonus, amyotrophy, unsteady gait, akinesia, rigidity, dysarthric speech) and intellectual deterioration. Muscle biopsy displays autofluorescent bodies and lipofuscin deposits in brain and, occasionally the retina, upon postmortem. |
Is a |
True |
Parkinsonism |
Inferred relationship |
Some |
|
A rare neurodegenerative disease characterized by extrapyramidal symptoms (rigidity, tremor, bradykinesia) and dementia, typically beginning in the fifth or sixth decade of life and progressing to a vegetative state with pelvicrural flexion contractures within few years. Oculomotor signs, olfactory dysfunction, and autonomic disturbances may also be observed. Neuropathological hallmarks are frontotemporally accentuated cerebral atrophy, as well as neurofibrillary tangles and neuronal loss in a characteristic distribution in cortical and subcortical regions. The disease is endemic to the Pacific Island of Guam. |
Is a |
True |
Parkinsonism |
Inferred relationship |
Some |
|
Progressive supranuclear palsy parkinsonism syndrome (disorder) |
Is a |
True |
Parkinsonism |
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 |
Parkinsonism |
Inferred relationship |
Some |
|
Amyotrophic lateral sclerosis with parkinsonism |
Is a |
True |
Parkinsonism |
Inferred relationship |
Some |
|
Amyotrophic lateral sclerosis, parkinsonism, dementia complex of Kii Peninsula (disorder) |
Is a |
True |
Parkinsonism |
Inferred relationship |
Some |
|
Amyotrophic lateral sclerosis, parkinsonism, dementia complex of West New Guinea (disorder) |
Is a |
True |
Parkinsonism |
Inferred relationship |
Some |
|
A rare parkinsonian syndrome due to neurodegenerative disease characterised by resting tremor (which may initially be asymmetric), rigidity, and bradykinesia. Polyneuropathy with neurogenic electromyography findings is present in the majority of the patients and reported in young age (early twenties) whereas parkinsonian symptoms are visible later in life (between 40 and 70 years of age). Additional clinical symptoms may include anxiety and depression. Mild diffuse muscular atrophy can also be detected in some patients. |
Is a |
True |
Parkinsonism |
Inferred relationship |
Some |
|
Frontotemporal dementia with parkinsonism-17 |
Is a |
True |
Parkinsonism |
Inferred relationship |
Some |
|