A late onset Parkinson disease that has material basis in heterozygous triplication of the alpha-synuclein gene (SNCA) on chromosome 4q22.
Comprehensive, easy-to-understand information about this condition
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Gene data from MyGene.info • Click to view on NCBI Gene
autosomal dominant Parkinson disease 1
MONDO:0008200
autosomal dominant Parkinson disease 8
MONDO:0011764
autosomal recessive Parkinson disease 14
MONDO:0013060
Parkinson disease 17
MONDO:0013625
Parkinson disease 21
MONDO:0014604
Parkinson disease 22, autosomal dominant
MONDO:0014742