ORPHA:657

Congenital isolated hyperinsulinism

Also called PHHI, Persistent hyperinsulinemic hypoglycemia of infancy

Body system

Inborn errors of metabolism

Inheritance pattern

Autosomal dominant, Autosomal recessive

Typical age of onset

Childhood, Infancy, Neonatal

Estimated prevalence

1-9 / 100 000 (Czech Republic)

Rarity class

1-9 / 100 000

ORPHA:657 is classified under "Inborn errors of metabolism" in the Orphanet nomenclature.