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Summary Literature (0)
MIM:601820 - HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 2; HHF2

Xenbase Genes: kcnj11

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011153 - hyperinsulinemic hypoglycemia, familial, 2
MONDO:0017185 - autosomal dominant hyperinsulinism due to Kir6.2 deficiency
MONDO:0017188 - diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency
MONDO:0019334 - autosomal recessive hyperinsulinism due to Kir6.2 deficiency

Disease Ontology (DO):
DOID:0070218 - familial hyperinsulinemic hypoglycemia 2
DOID:13317 - hyperinsulinemic hypoglycemia