recurrent hypoglycemia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Recurrent episodes of decreased concentration of glucose in the blood. (Human Phenotype Ontology, HP_0001988)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001988
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Genes

3 genes associated with the recurrent hypoglycemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
MC2R melanocortin 2 receptor (adrenocorticotropic hormone)
MRAP melanocortin 2 receptor accessory protein
SLC22A5 solute carrier family 22 (organic cation/carnitine transporter), member 5