disease has basis in dysfunction of SLC2A2 glycogen storage disease glycogen storage disease due to GLUT2 deficiency Bickel-Fanconi glycogenosis FBS Fanconi Bickel syndrome Fanconi syndrome with intestinal malabsorption and galactose intolerance Fanconi-Bickel disease 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. Fanconi-Bickel syndrome GARD:0002268 GLUT2 deficiency GSD due to GLUT2 deficiency GSD type 11 GSD type XI ICD10:E74.0 MONDO:0009216 OMIM:227810 Orphanet:2088 SCTID:61598006 glycogen storage disease 11 glycogen storage disease XI glycogen storage disease due to GLUT2 deficiency glycogen storage disease type 11 glycogen storage disease type XI glycogenosis Fanconi EXACT glycogenosis due to GLUT2 deficiency glycogenosis, Fanconi type hepatic glycogenosis with Fanconi nephropathy hepatic glycogenosis with amino aciduria and glucosuria hepatorenal glycogenosis with renal Fanconi syndrome hepatorenal glycogenosis with renal fanconi syndrome https://rarediseases.info.nih.gov/diseases/2268/fanconi-bickel-syndrome pseudo-phlorizin diabetes glucose transport disorder nephropathy secondary to a storage or other metabolic disease