Conversion Disorder Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A somatoform disorder that involves numbness, blindness, paralysis or fits without a neurological cause. (Human Disease Ontology, DOID_1768)
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Genes

1 genes associated with the Conversion Disorder phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
COMT catechol-O-methyltransferase