PedAM
Pediatric Disease Annotations & Medicines
| Disease | lysosomal storage disease |
| Phenotype | C0017921|acid alpha-glucosidase deficiency |
| Sentences | 1 |
| PubMedID- 20875764 | Background: pompe disease (acid alpha-glucosidase deficiency) is one of several lysosomal storage diseases amenable to treatment with enzyme replacement therapy (ert). |
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