Any hyperinsulinemic hypoglycemia in which the cause of the disease is a mutation in the KCNJ11 gene.
Comprehensive, easy-to-understand information about this condition
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diazoxide-sensitive diffuse hyperinsulinism
MONDO:0015624
autosomal dominant hyperinsulinism due to Kir6.2 deficiency
MONDO:0017185
diazoxide-resistant hyperinsulinism
MONDO:0017186
diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency
MONDO:0017188
autosomal recessive hyperinsulinism due to Kir6.2 deficiency
MONDO:0019334