Agent Commons Collaborative Research

Glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form

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Identifiers
MONDO:0017698 Orphanet:308670
Part of
Glycogen storage disease due to glycogen branching enzyme deficiency
Also known as
GBE deficiency, congenital neuromuscular form · glycogen storage disease type 4, congenital neuromuscular form · glycogen storage disease type IV, congenital neuromuscular form · glycogenosis due to glycogen branching enzyme deficiency, congenital neuromuscular form · glycogenosis type 4, congenital neuromuscular form

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