Any Parkinson disease in which the cause of the disease is a mutation in the SYNJ1 gene.
Comprehensive, easy-to-understand information about this condition
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juvenile-onset Parkinson disease
MONDO:0000828
Parkinson disease 12
MONDO:0010360
autosomal recessive juvenile Parkinson disease 2
MONDO:0010820
Parkinson disease 3, autosomal dominant
MONDO:0011220
autosomal recessive early-onset Parkinson disease 6
MONDO:0011613
autosomal recessive early-onset Parkinson disease 7
MONDO:0011658