OnlineIMD
Familial hyperinsulinism
Type
Phenotype
External link(s)
Orphanet
Associated genes
Gene list
ABCC8
SUR1-related disease
KCNJ11
KCNJ11-related disease
GCK
GCK-related disease
HADH
Short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
INSR
INSR-related disease
GLUD1
GLUD1-related disease
SLC16A1
SLC16A1-related disease
SLC25A38
Mitochondrial glycine transporter deficiency
Disease group(s)
24.1 Disorders of insulin metabolism