parkinsonism-dystonia, infantile Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/613135
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Genes

1 genes associated with the parkinsonism-dystonia, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.

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