Agent Commons Collaborative Research

Diazoxide-sensitive diffuse hyperinsulinism

rare

Identifiers: MONDO:0015624 Orphanet:165985
Part of: Congenital isolated hyperinsulinism
Also known as: hyperinsulinemic hypoglycemia, diazoxide-sensitive diffuse form

Subtypes

All diseases Rare only

Disease	ID	Subtypes	Genes
Autosomal dominant hyperinsulinism due to Kir6.2 deficiency	MONDO:0017185
Autosomal dominant hyperinsulinism due to SUR1 deficiency	MONDO:0017184
Exercise-induced hyperinsulinism	MONDO:0012396		SLC16A1
Hyperinsulinemic hypoglycemia, familial, 4	MONDO:0012382		HADH
Hyperinsulinism due to HNF1A deficiency	MONDO:0017935
Hyperinsulinism due to HNF4A deficiency	MONDO:0016988
Hyperinsulinism due to UCP2 deficiency	MONDO:0017183
Hyperinsulinism-hyperammonemia syndrome	MONDO:0011717		GLUD1

Rare disease

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