ORPHA:420429

Glycogen storage disease due to acid maltase deficiency, late-onset

Also called Alpha-1,4-glucosidase acid deficiency, late-onset, GSD due to acid maltase deficiency, late-onset, GSD type 2, late-onset, GSD type II, late-onset, Glycogen storage disease type 2, late-onset, Glycogen storage disease type II, late-onset, Glycogenosis type 2, late-onset, Glycogenosis type II, late-onset, Pompe disease, late-onset

Body system

Inborn errors of metabolism

Inheritance pattern

Autosomal recessive

Typical age of onset

Adolescent, Adult

Estimated prevalence

1-9 / 100 000 (Worldwide)

Rarity class

1-9 / 100 000

ORPHA:420429 is classified under "Inborn errors of metabolism" in the Orphanet nomenclature.