Parkinsonism-Dystonia, Infantile Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C567730
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Genes

1 genes/proteins associated with the disease Parkinsonism-Dystonia, Infantile from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
SLC6A3 solute carrier family 6 (neurotransmitter transporter), member 3 2.88009