hallucinations Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Perceptions in a conscious and awake state in the absence of external stimuli which have qualities of real perception, in that they are vivid, substantial, and located in external objective space. (Human Phenotype Ontology, HP_0000738)
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5 genes associated with the disease hallucinations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
COMT catechol-O-methyltransferase
GABRB3 gamma-aminobutyric acid (GABA) A receptor, beta 3
MAOB monoamine oxidase B
PAH phenylalanine hydroxylase
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4