Hyperinsulinemic hypoglycemia, familial, 1

MONDO:0009734

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

Also known as: ABCC8 hyperinsulinemic hypoglycemia (disease), hyperinsulinemic hypoglycemia (disease) caused by mutation in ABCC8, hyperinsulinemic hypoglycemia due to SUR1 deficiency, hyperinsulinemic hypoglycemia, familial, 1, hyperinsulinemic hypoglycemia, familial, type 1, HHF1, Nesidioblastosis of pancreas, hyperinsulinemic hypoglycemia due to focal adenomatous hyperplasia

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

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Where it sits in the disease tree

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↑ Hyperinsulinemic hypoglycemia (14)

Sub-types of Hyperinsulinemic hypoglycemia, familial, 1

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

Where it sits in the disease tree

Newborn screening study aims to catch rare diseases at birth