glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form

Rare Disease

MONDO:0017699

Also known as:

GBE deficiency, childhood combined hepatic and myopathic formGSD due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic formGSD type 4, childhood combined hepatic and myopathic form

Genes

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Clinical Trials

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Newborn Screening

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Patient Groups

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