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Fanconi-bickel syndrome
Fanconi-bickel syndrome
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Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
FANCONI-BICKEL SYNDROME
2088
227810
C3495427
SLC2A2
Causal
21327337
22865906
ClinVar
,
Disgenet
,
HPO
,
Orphanet
Insulin secretion
Prolactin signaling pathway
Glucagon signaling pathway
Type II diabetes mellitus
Insulin resistance
Maturity onset diabetes of the young
Carbohydrate digestion and absorption
Central carbon metabolism in cancer
Cellular hexose transport
Regulation of insulin secretion
Defective SLC2A2 causes Fanconi-Bickel syndrome (FBS)
Intestinal hexose absorption
+9 more
LDHA
Unknown
—
Disgenet
Glycolysis / Gluconeogenesis
Cysteine and methionine metabolism
Pyruvate metabolism
Propanoate metabolism
Metabolic pathways
HIF-1 signaling pathway
Glucagon signaling pathway
Central carbon metabolism in cancer
Pyruvate metabolism
+6 more
All
2
Causal
1
Unknown
1
Select all
Clear
ClinVar
1
Orphanet
1
Disgenet
2
CTD
0
HPO
1
GWAS catalog
0
GenCC
0
ClinGen
0
Related Diseases
Diseases that share the most curated genes with Fanconi-bickel syndrome.
5
View disease cluster →
Fanconi syndrome
1 shared gene
SLC2A2
Related via 1 shared gene including SLC2A2.
Transient neonatal diabetes mellitus
1 shared gene
SLC2A2
Related via 1 shared gene including SLC2A2.
Permanent neonatal diabetes mellitus
1 shared gene
SLC2A2
Related via 1 shared gene including SLC2A2.
Glycogen storage disease
2 shared genes
LDHA, SLC2A2
Related via 2 shared genes including LDHA, SLC2A2.
Neonatal diabetes mellitus
1 shared gene
SLC2A2
Related via 1 shared gene including SLC2A2.
1
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