Parkinsonian disorder
MONDO:0021095A group of disorders which feature impaired motor control characterized by bradykinesia, MUSCLE RIGIDITY; TREMOR; and postural instability. Parkinsonian diseases are generally divided into primary parkinsonism (see PARKINSON DISEASE), secondary parkinsonism (see PARKINSON DISEASE, SECONDARY) and inherited forms. These conditions are associated with dysfunction of dopaminergic or closely related motor integration neuronal pathways in the BASAL GANGLIA.
1315 clinical trials for this condition and its sub-types, 67 tagged with Parkinsonian disorder itself.
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Sub-types of Parkinsonian disorder
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Parkinson disease 1,169 trials · 1,296 incl. sub-types
6 sub-types
- Late-onset Parkinson disease 3 trials · 143 incl. sub-types Sub-types →
- Young-onset Parkinson disease 9 trials · 11 incl. sub-types Sub-types →
- Parkinson disease 16 0 trials
- Parkinson disease 25, autosomal recessive early-onset, with impaired intellectual development 0 trials
- Parkinson disease, mitochondrial 0 trials
- Parkinsonian-pyramidal syndrome 0 trials Sub-types →
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Vascular parkinsonism 4 trials
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Dystonia 12 2 trials
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Perry syndrome 0 trials
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X-linked dystonia-parkinsonism 0 trials
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Atypical juvenile parkinsonism 0 trials
1 sub-type
- Juvenile onset Parkinson disease 19A 0 trials
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Cyanide-induced parkinsonism 0 trials
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Dystonia 16 0 trials
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Encephalitis lethargica 0 trials
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Parkinsonism with polyneuropathy 0 trials
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Parkinsonism-dystonia, infantile 0 trials
3 sub-types
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Postencephalitic Parkinson disease 0 trials
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Primary progressive freezing gait 0 trials
Most studied deeper sub-types
Autosomal dominant Parkinson disease 4
(136)
Autosomal recessive early-onset Parkinson disease 6
(4)
Autosomal dominant Parkinson disease 1
(3)
Autosomal recessive juvenile Parkinson disease 2
(2)
Autosomal dominant Parkinson disease 8
(1)
Autosomal recessive early-onset Parkinson disease 7
(1)
Autosomal recessive early-onset Parkinson disease 23
(0)
Autosomal recessive Parkinson disease 14
(0)
Early-onset Parkinson disease 20
(0)
Juvenile-onset Parkinson disease
(0)
Kufor-Rakeb syndrome
(0)
Paralysis agitans, juvenile, of Hunt
(0)
Parkinson disease 10
(0)
Parkinson disease 12
(0)
Parkinson disease 17
(0)
Parkinson disease 19B, early-onset
(0)
Parkinson disease 21
(0)
Parkinson disease 22, autosomal dominant
(0)
Parkinson disease 3, autosomal dominant
(0)
Parkinsonism due to ATP13A2 deficiency
(0)