Human Disease and Mouse Model Detail
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Human Disease
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Fanconi-Bickel Syndrome; FBS
OMIM ID: 227810
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Synonyms
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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
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Genes and
mouse models
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Mutations in human and/or mouse homologs are associated with this disease
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*Gene is associated with the disease in this species |
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Slc2a2
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SLC2A2*
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1:1 Homology
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Analysis Tools