hyperinsulinemic hypoglycemia Gene Set

Dataset HPO Gene-Disease 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)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000825
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Genes

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

Symbol Name
ABCC8 ATP-binding cassette, sub-family C (CFTR/MRP), member 8
GCK glucokinase (hexokinase 4)
GLUD1 glutamate dehydrogenase 1
HADH hydroxyacyl-CoA dehydrogenase
INSR insulin receptor
KCNJ11 potassium channel, inwardly rectifying subfamily J, member 11
MPI mannose phosphate isomerase
SLC16A1 solute carrier family 16 (monocarboxylate transporter), member 1
TRMT10A tRNA methyltransferase 10 homolog A (S. cerevisiae)