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Summary Literature (0)
MIM:613135 - PARKINSONISM-DYSTONIA 1, INFANTILE-ONSET; PKDYS1

Xenbase Genes: slc6a3

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0054835 - classic dopamine transporter deficiency syndrome

Disease Ontology (DO):
DOID:0070489 - classic dopamine transporter deficiency syndrome