Any hyperinsulinemic hypoglycemia in which the cause of the disease is a mutation in the ABCC8 gene.
Comprehensive, easy-to-understand information about this condition
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familial hyperinsulinism
MONDO:0017182
diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency
MONDO:0017187
insulin autoimmune syndrome
MONDO:0018465
autosomal recessive hyperinsulinism due to SUR1 deficiency
MONDO:0019333
hyperinsulinemic hypoglycemia, familial, 8
MONDO:0859362
hyperinsulinemic hypoglycemia with polycystic kidney disease
MONDO:1030000