has material basis in germline mutation in SLC2A2 disorder of glycogen metabolism glycogen storage disease due to GLUT2 deficiency https://github.com/monarch-initiative/mondo/issues/4985 https://github.com/monarch-initiative/mondo/issues/9285 https://rarediseases.info.nih.gov/diseases/2268/fanconi-bickel-syndrome https://www.malacards.org/card/fanconi_bickel_syndrome GSD type XI MONDO:0009216 GARD:0002268 MEDGEN:501176 Fanconi Bickel syndrome OMIM:227810 glycogenosis due to GLUT2 deficiency hepatorenal glycogenosis with renal fanconi syndrome hepatic glycogenosis with amino aciduria and glucosuria glycogen storage disease type 11 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. GSD due to GLUT2 deficiency glycogenosis Fanconi EXACT pseudo-phlorizin diabetes Orphanet:2088 hepatorenal glycogenosis with renal Fanconi syndrome GSD type 11 Fanconi-Bickel syndrome Fanconi syndrome with intestinal malabsorption and galactose intolerance glycogen storage disease type XI glycogen storage disease due to GLUT2 deficiency glycogen storage disease XI Bickel-Fanconi glycogenosis FBS SCTID:61598006 icd11.foundation:426701963 glycogen storage disease 11 GLUT2 deficiency DOID:0070562 UMLS:C3495427 disorder of carbohydrate transmembrane transport and absorption glucose transport disorder obsolete nephropathy secondary to a storage or other metabolic disease