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

1 clinical trial for this condition and its sub-types, 1 tagged with Hyperinsulinemic hypoglycemia, familial, 2 itself.

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Where it sits in the disease tree

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↑ Congenital isolated hyperinsulinism (2)

Sub-types of Hyperinsulinemic hypoglycemia, familial, 2

Including sub-types (1) Tagged with Hyperinsulinemic hypoglycemia, familial, 2 (1)

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Newborn screening study aims to catch rare diseases at birth

Diagnosis Ongoing

This study offers voluntary screening for newborns in North Carolina to detect a wide range of rare health conditions early. Using a small blood sample already collected at birth, the program tests for dozens of disorders, including spinal muscular atrophy, cystic fibrosis, and m…

Sponsor: RTI International • Aim: Diagnosis

Last updated Jul 03, 2026 00:00 UTC

Hyperinsulinemic hypoglycemia, familial, 2

Where it sits in the disease tree

Newborn screening study aims to catch rare diseases at birth