Bulimia Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A form of anomalous eating behavior characterized by binge eating is followed by self-induced vomiting or other compensatory behavior intended to prevent weight gain (purging, fasting or exercising or a combination of these). (Human Phenotype Ontology, HP_0100739)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D002032
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Genes

3 genes/proteins associated with the disease Bulimia from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
BDNF brain-derived neurotrophic factor 1.24655
CYP3A4 cytochrome P450, family 3, subfamily A, polypeptide 4 1.04647
SLC22A2 solute carrier family 22 (organic cation transporter), member 2 1.01549