persistent hyperinsulinemia hypoglycemia of infancy Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A carbohydrate metabolic disorder that involves low blood glucose resulting from an excess of insulin. (Human Disease Ontology, DOID_13317)
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Genes

3 genes associated with the disease persistent hyperinsulinemia hypoglycemia of infancy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ABCC8 ATP-binding cassette, sub-family C (CFTR/MRP), member 8
GCK glucokinase (hexokinase 4)
KCNJ11 potassium channel, inwardly rectifying subfamily J, member 11