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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

30 clinical trials for this condition and its sub-types.

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Sub-types

Autosomal recessive hyperinsulinism due to SUR1 deficiency (0) Diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency (0)

Broader categories

Disease (618) Metabolic disease (215) Hereditary disease (172) Endocrine system disorder (61) Inborn errors of metabolism (42) Human disease (14) Carbohydrate metabolism disease (3) Disease of genetic or genomic mechanism (2) Hyperinsulinemic hypoglycemia (2) Inborn carbohydrate metabolic disorder (2)

Trials to join now! 16 Not yet recruiting 3 Not yet finished but already full! 5 Completed 6

Hyperinsulinemic hypoglycemia, familial, 1

Sub-types

Broader categories

Newborn screening study aims to catch rare diseases at birth

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