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Human Disease and Mouse Model Detail
Human Disease

Term: Fanconi-Bickel Syndrome; FBS
OMIM ID: 227810

Synonyms Fanconi Syndrome with Intestinal Malabsorption and Galactose Intolerance; Glycogenosis, Fanconi Type; Glycogen Storage Disease XI; Hepatic Glycogenosis with Amino Aciduria and Glucosuria; Hepatic Glycogenosis with Fanconi Nephropathy; Hepatorenal Glycogenosis with Renal Fanconi Syndrome; Pseudo-Phlorizin Diabetes
Associated Genes

Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.

Mouse Gene
Human Gene
 
Characteristics of this human disease are associated with mutations in...
     
Slc2a2 SLC2A2
  human...the human gene.
     MGI data currently do not associate this disease with mutations in the orthologous mouse gene.
     
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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Send questions and comments to User Support. 		last database update
04/03/2013
MGI 5.12 		The Jackson Laboratory