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Glycogen storage disease due to GLUT2 deficiency
rareFanconi-Bickel glycogenosis (FBG) is a rare glycogen storage disease characterized by hepatorenal glycogen accumulation, severe renal tubular dysfunction and impaired glucose and galactose metabolism.
- Identifiers
- MONDO:0009216 OMIM:227810Orphanet:2088
- Causal genes
- SLC2A2
- Part of
- Disorder of glycogen metabolism
- Also known as
- Bickel-Fanconi glycogenosis · Fanconi Bickel syndrome · Fanconi syndrome with intestinal malabsorption and galactose intolerance · Fanconi-Bickel disease · Fanconi-Bickel syndrome
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