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Human Disease and Mouse Model Detail
Human Disease Fanconi-Bickel Syndrome; FBS
OMIM ID: 227810
Human Phenotype Ontology associations
Synonyms Fanconi Syndrome with Intestinal Malabsorption and Galactose Intolerance; Glycogen Storage Disease XI; Glycogenosis, Fanconi Type; Hepatic Glycogenosis with Amino Aciduria and Glucosuria; Hepatic Glycogenosis with Fanconi Nephropathy; Hepatorenal Glycogenosis with Renal Fanconi Syndrome; Pseudo-Phlorizin Diabetes
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     SLC2A2* Slc2a2   HomoloGene and HGNC

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.07
The Jackson Laboratory