Patient Engagement Synapse - Condition

A progressive degenerative disorder of the central nervous system characterized by loss of dopamine producing neurons in the substantia nigra and the presence of Lewy bodies in the substantia nigra and locus coeruleus. Signs and symptoms include tremor which is most pronounced during rest, muscle rigidity, slowing of the voluntary movements, a tendency to fall back, and a mask-like facial expression.

Synonyms

Parkinson's disease , paralysis agitans

Related diseases

CHCHD2 Parkinson disease , CLN12 disease , DNAJC13 hereditary late onset Parkinson disease , DNAJC6 Parkinson disease , EIF4G1 hereditary late onset Parkinson disease , GIGYF2 hereditary late onset Parkinson disease , Kufor-Rakeb syndrome , LOPD , LRRK2 Parkinson disease , PARK10 , PARK12 , PARK14 , PARK16 , PARK22 , PARK23 , PARK3 , PARK7 Parkinson disease , PARK9 , PINK1 Parkinson disease , PLA2G6 hereditary late onset Parkinson disease , PLA2G6-related dystonia-parkinsonism , PRKN young-onset Parkinson disease , Pallidopyramidal syndrome , Parkinson disease 11, autosomal dominant, susceptibility to , Parkinson disease 17 , Parkinson disease 18, autosomal dominant, susc Display more information eptibility to , Parkinson disease 21 , Parkinson disease 22, autosomal dominant , Parkinson disease 22, autosomal dominant; PARK22 , Parkinson disease 23, autosomal recessive early-onset , Parkinson disease 5, autosomal dominant, susceptibility to , Parkinson disease caused by mutation in CHCHD2 , Parkinson disease caused by mutation in DNAJC6 , Parkinson disease caused by mutation in LRRK2 , Parkinson disease caused by mutation in PARK7 , Parkinson disease caused by mutation in PINK1 , Parkinson disease caused by mutation in SYNJ1 , Parkinson disease caused by mutation in VPS35 , Parkinson disease type 17 , Parkinson disease type 21 , Parkinson disease, mitochondrial , SYNJ1 Parkinson disease , UCHL1 young-onset Parkinson disease , VPS13C young-onset Parkinson disease , VPS35 Parkinson disease , YOPD , autosomal dominant Lewy body Parkinson disease 4 , autosomal dominant Parkinson disease 1 , autosomal dominant Parkinson disease 17 , autosomal dominant Parkinson disease 4 , autosomal dominant Parkinson disease 8 , autosomal dominant Parkinson disease type 1 , autosomal dominant Parkinson disease type 4 , autosomal dominant Parkinson disease type 8 , autosomal dominant late-onset Parkinson disease , autosomal recessive Parkinson disease 14 , autosomal recessive Parkinson disease 9 , autosomal recessive Parkinson disease type 14 , autosomal recessive early-onset Parkinson disease 15 , autosomal recessive early-onset Parkinson disease 23 , autosomal recessive early-onset Parkinson disease 6 , autosomal recessive early-onset Parkinson disease 7 , autosomal recessive early-onset Parkinson disease type 15 , autosomal recessive early-onset Parkinson disease type 6 , autosomal recessive early-onset Parkinson disease type 7 , autosomal recessive early-onset Parksinson disease 23 , autosomal recessive early-onset Parksinson disease type 23 , autosomal recessive juvenile Parkinson disease 2 , autosomal recessive juvenile Parkinson disease type 2 , autosomal recessive juvenile onset Parkinson disease 9 , dystonia-Parkinsonism Adult-onset , dystonia-parkinsonism, Paisan-Ruiz type , early-onset Parkinson disease , early-onset Parkinson disease 20 , early-onset Parkinson disease 6 , early-onset Parkinson disease type 20 , hereditary late onset Parkinson disease , hereditary late onset Parkinson disease caused by mutation in DNAJC13 , hereditary late onset Parkinson disease caused by mutation in EIF4G1 , hereditary late onset Parkinson disease caused by mutation in GIGYF2 , hereditary late onset Parkinson disease caused by mutation in PLA2G6 , juvenile onset Parkinson disease 19A , juvenile onset Parkinson disease type 19A , juvenile-onset Parkinson disease , late-onset Parkinson disease , pallidopyramidal syndrome , paralysis agitans, juvenile, of Hunt , parkinsonian-pyramidal syndrome , parkinsonism due to ATP13A2 deficiency , young-onset Parkinson disease , young-onset Parkinson disease caused by mutation in PRKN , young-onset Parkinson disease caused by mutation in UCHL1 , young-onset Parkinson disease caused by mutation in VPS13C

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