Familial hyperinsulinism
MONDO:0017182An instance of hyperinsulinism (disease) that is caused by an inherited modification of the individual's genome.
Also known as: hyperinsulinemic hypoglycemia, FHI, HHI, congenital hyperinsulinism, familial hyperinsulinemic hypoglycemia, hereditary hyperinsulinism (disease), hyperinsulinemia of infancy, neonatal hyperinsulinism
12 clinical trials for this condition and its sub-types, 9 tagged with Familial hyperinsulinism itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Familial hyperinsulinism
-
Congenital isolated hyperinsulinism 0 trials · 2 incl. sub-types
4 sub-types
- Diazoxide-sensitive diffuse hyperinsulinism 0 trials · 2 incl. sub-types Sub-types →
- Hyperinsulinemic hypoglycemia, familial, 2 1 trial Sub-types →
- Diazoxide-resistant hyperinsulinism 0 trials Sub-types →
- Hyperinsulinemic hypoglycemia, familial, 3 0 trials
Most studied deeper sub-types
Exercise-induced hyperinsulinism
(1)
Hyperinsulinism-hyperammonemia syndrome
(1)
Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
(0)
Autosomal dominant hyperinsulinism due to SUR1 deficiency
(0)
Autosomal recessive hyperinsulinism due to Kir6.2 deficiency
(0)
Autosomal recessive hyperinsulinism due to SUR1 deficiency
(0)
Diazoxide-resistant diffuse hyperinsulinism
(0)
Diazoxide-resistant focal hyperinsulinism
(0)
Diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency
(0)
Diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency
(0)
Hyperinsulinemic hypoglycemia, familial, 4
(0)
Hyperinsulinism due to HNF1A deficiency
(0)
Hyperinsulinism due to HNF4A deficiency
(0)
Hyperinsulinism due to UCP2 deficiency
(0)