ORPHA:2116

Hartnup disease

Also called Aminoaciduria, Hartnup type, Hartnup disorder

Body system

Inborn errors of metabolism

Inheritance pattern

Autosomal recessive

Typical age of onset

All ages

Estimated prevalence

1-9 / 100 000 (United States)

Rarity class

1-9 / 100 000

ORPHA:2116 is classified under "Inborn errors of metabolism" in the Orphanet nomenclature.