Parkinson's disease , paralysis agitans

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 Display less info