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Home/Rare disease/Glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form

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

ORPHA:308684· ICD-10 E74.0

Inheritance: Autosomal recessive

ICD-10 E74.0 →

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Not medical advice. Consult a healthcare professional. This information is general reference based on public data and does not replace consultation with a doctor or pharmacist.

Source:

Orphanet — Orphanet Rare Disease Nomenclature (CC BY 4.0) [Source data]

Source: Orphanet (orpha.net) — used under CC BY 4.0.

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