Hyperphagia Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A neurological anomaly with gross overeating associated with an abnormally strong desire or need to eat. (Human Phenotype Ontology, HP_0002591)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D006963
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Genes

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

Symbol Name Standardized Value
LEP leptin 2.88009
LEPR leptin receptor 2.88009
MC4R melanocortin 4 receptor 2.88009
NTRK2 neurotrophic tyrosine kinase, receptor, type 2 2.88009