Dyskinesia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A movement disorder which consists of effects including diminished voluntary movements and the presence of involuntary movements. (Human Phenotype Ontology, HP_0100660)
External Link https://www.disgenet.org/browser/0/1/0/C4310683
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Genes

2 genes associated with the disease Dyskinesia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
DEAF1 DEAF1 transcription factor
PDE10A phosphodiesterase 10A