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hyperinsulinemic hypoglycemia, familial, 1

Disease Summary
Associated Targets (3)
Tclin

2

Tchem

1


Mondo Description Any hyperinsulinemic hypoglycemia in which the cause of the disease is a mutation in the ABCC8 gene.
Uniprot Description Most common cause of persistent hypoglycemia in infancy. Unless early and aggressive intervention is undertaken, brain damage from recurrent episodes of hypoglycemia may occur.
Mondo Term and Equivalent IDs
MONDO:0009734:  hyperinsulinemic hypoglycemia, familial, 1
SCTID:360339005: