ORPHA:3057

Monoamine oxidase A deficiency

Also called Brunner syndrome

Body system

Inborn errors of metabolism

Inheritance pattern

X-linked recessive

Typical age of onset

Childhood

Estimated prevalence

Unknown (Worldwide)

Rarity class

Unknown

ORPHA:3057 is classified under "Inborn errors of metabolism" in the Orphanet nomenclature.