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Glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form
rare- Identifiers
- MONDO:0017699 Orphanet:308684
- Also known as
- GBE deficiency, childhood combined hepatic and myopathic form · glycogen storage disease type 4, childhood combined hepatic and myopathic form · glycogen storage disease type IV, childhood combined hepatic and myopathic form · glycogenosis due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form · glycogenosis type 4, childhood combined hepatic and myopathic form
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