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hyperinsulinemic hypoglycemia, familial, 1

The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

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Disease Overview

Any hyperinsulinemic hypoglycemia in which the cause of the disease is a mutation in the ABCC8 gene.

Synonyms

  • ABCC8 hyperinsulinemic hypoglycemia (disease)
  • HHF1
  • Nesidioblastosis of pancreas
  • hyperinsulinemic hypoglycemia (disease) caused by mutation in ABCC8
  • hyperinsulinemic hypoglycemia due to SUR1 deficiency
  • hyperinsulinemic hypoglycemia due to focal adenomatous hyperplasia
  • hyperinsulinemic hypoglycemia, familial, 1
  • hyperinsulinemic hypoglycemia, familial, type 1
  • hyperinsulinism, congenital
  • hyperinsulinism, familial, with pancreatic Nesidioblastosis
  • hypoglycemia, hyperinsulinemic, of infancy
  • persistent hyperinsulinemic hypoglycemia of infancyABCC8 hyperinsulinemic hypoglycemia (disease)
  • HHF1
  • Nesidioblastosis of pancreas
  • hyperinsulinemic hypoglycemia (disease) caused by mutation in ABCC8
  • hyperinsulinemic hypoglycemia due to SUR1 deficiency
  • hyperinsulinemic hypoglycemia due to focal adenomatous hyperplasia
  • hyperinsulinemic hypoglycemia, familial, 1
  • hyperinsulinemic hypoglycemia, familial, type 1
  • hyperinsulinism, congenital
  • hyperinsulinism, familial, with pancreatic Nesidioblastosis
  • hypoglycemia, hyperinsulinemic, of infancy
  • persistent hyperinsulinemic hypoglycemia of infancy
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