Hyperinsulinemic hypoglycemia, familial, 2

MONDO:0011153

Any hyperinsulinemic hypoglycemia in which the cause of the disease is a mutation in the KCNJ11 gene.

Also known as: KCNJ11 hyperinsulinemic hypoglycemia (disease), hyperinsulinemic hypoglycemia (disease) caused by mutation in KCNJ11, hyperinsulinemic hypoglycemia due to Kir6.2 deficiency, hyperinsulinemic hypoglycemia, familial, 2, hyperinsulinemic hypoglycemia, familial, type 2, HHF2, hyperinsulinemic hypoglycemia due to focal adenomatous hyperplasia, hyperinsulinemic hypoglycemia familial 2

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