Familial hyperinsulinism

rare

An instance of hyperinsulinism (disease) that is caused by an inherited modification of the individual's genome.

Identifiers: MONDO:0017182 Orphanet:276525
Part of: Hyperinsulinemic hypoglycemia Hyperinsulinism
Also known as: congenital hyperinsulinism · familial hyperinsulinemic hypoglycemia · FHI · hereditary hyperinsulinism (disease) · HHI

Subtypes

Disease	ID	Subtypes	Genes
Congenital isolated hyperinsulinism	MONDO:0019010	18
Adult-onset non-insulinoma persistent hyperinsulinemic hypoglycemia	MONDO:0017189
Hyperinsulinism due to INSR deficiency	MONDO:0012381		INSR

Rare disease

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