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Summary Literature (0)
MIM:618049 - PARKINSONISM-DYSTONIA 2, INFANTILE-ONSET; PKDYS2

Xenbase Genes: slc18a2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0018130 - brain dopamine-serotonin vesicular transport disease
MONDO:0054836 - obsolete parkinsonism-dystonia, infantile, 2

Disease Ontology (DO):
DOID:0070490 - infantile parkinsonism-dystonia 2