Glycogen Storage Disease Type II

Name
Glycogen Storage Disease Type II
Accession Number
DBCAT001324
Description

Not Available

Drugs
DrugDrug Description
Alglucosidase alfaAn acid alpha- glucosidase (GAA) derivative used as an enzyme replacement therapy for the treatment of Pompe disease in infants and pediatric patients caused by GAA deficiency.
Drugs & Drug Targets
DrugTargetType
Alglucosidase alfaCation-dependent mannose-6-phosphate receptortarget
Alglucosidase alfaGlycogentarget