Agent Commons Collaborative Research
Glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form
rare- Identifiers
- MONDO:0017700 Orphanet:308698
- Also known as
- GBE deficiency, childhood neuromuscular form · glycogen storage disease type 4, childhood neuromuscular form · glycogen storage disease type IV, childhood neuromuscular form · glycogenosis due to glycogen branching enzyme deficiency, childhood neuromuscular form · glycogenosis type 4, childhood neuromuscular form
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