dystonia-12 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Rapid-onset dystonia-parkinsonism (RDP) is a very rare movement disorder, characterized by the abrupt onset of parkinsonism and dystonia, often triggered by physical or psychological stress. (Orphanet Rare Disease Ontology, Orphanet_71517)
External Link http://www.omim.org/entry/128235
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1 genes associated with the dystonia-12 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
ATP1A3 ATPase, Na+/K+ transporting, alpha 3 polypeptide