MONDO_0009216 (glycogen storage disease due to GLUT2 deficiency) can be described as follows. Fanconi-Bickel glycogenosis (FBG) is a rare glycogen storage disease characterized by hepatorenal glycogen accumulation, severe renal tubular dysfunction and impaired glucose and galactose metabolism. Also known as: Bickel-Fanconi glycogenosis, FBS, Fanconi Bickel syndrome, Fanconi syndrome with intestinal malabsorption and galactose intolerance, Fanconi-Bickel disease, Fanconi-Bickel syndrome, GSD due to GLUT2 deficiency, glycogenosis due to GLUT2 deficiency.