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Parkinsonian disorder

MONDO:0021095

A 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.

1312 clinical trials for this condition and its sub-types, 67 tagged with Parkinsonian disorder itself.

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Part of

↑ Basal ganglia disorder (1319)

Sub-types of Parkinsonian disorder

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)
Including sub-types (1312) Tagged with Parkinsonian disorder (67)
Trials to join now! 24 Not yet recruiting 10 Not yet finished but already full! 13 Completed 19 Terminated 1
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