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PedAM

Pediatric Disease Annotations & Medicines




Disease lysosomal storage disease
Phenotype C0017921|glycogen storage disease type ii
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PubMedID- 24642446 Pompe disease (pd), which is also called glycogen storage disease type ii (gsdii), is one of the lysosomal storage diseases (lsds) caused by a deficiency in acid-alpha-glucosidase (gaa) in the lysosome and is characterized by the accumulation of glycogen in various cells.

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