Hyperinsulinemic hypoglycemia, familial, 1
MONDO:0009734Any 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.
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Broader categories
Disease
(717)
Metabolic disease
(241)
Hereditary disease
(188)
Endocrine system disorder
(78)
Inborn errors of metabolism
(47)
Human disease
(15)
Carbohydrate metabolism disease
(4)
Disease of genetic or genomic mechanism
(2)
Hyperinsulinemic hypoglycemia
(2)
Inborn carbohydrate metabolic disorder
(2)