ORPHA:727719
Monoamine oxidase A and monoamine oxidase B deficiency
Also called Monoamine oxidase A and monoamine oxidase B deletion syndrome, MAOA/B deletion syndrome, MAOA/B deficiency
- Body system
- Inborn errors of metabolism
- Inheritance pattern
- X-linked recessive
- Typical age of onset
- Childhood, Infancy
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:727719 is classified under "Inborn errors of metabolism" in the Orphanet nomenclature.