Persistent Hyperinsulinemia Hypoglycemia of Infancy Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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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5 genes associated with the Persistent Hyperinsulinemia Hypoglycemia of Infancy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ABCC8 ATP-binding cassette, sub-family C (CFTR/MRP), member 8
GCK glucokinase (hexokinase 4)
GLUD1 glutamate dehydrogenase 1
HNF4A hepatocyte nuclear factor 4, alpha
KCNJ11 potassium channel, inwardly rectifying subfamily J, member 11