Fructose metabolism

Pathway network for the Fructose metabolism SuperPath

Sources:
  • Reactome
  • WikiPathways
  • PubChem

Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways

Disorders associated with Fructose metabolism SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Glycogen storage disease iaDirect
2Fructose intolerance, hereditaryDirect
3Neuronopathy, distal hereditary motor, autosomal recessive 8EnrichmentSORD4.13
4Fructosuria, essentialEnrichmentKHK3.53
5D-glyceric aciduriaEnrichmentGLYCTK3.43
6Triokinase and fmn cyclase deficiency syndromeEnrichmentTKFC3.43
7Inherited metabolic disorderEnrichmentTKFC3.43
8Anemia, congenital, nonspherocytic hemolytic, 5EnrichmentHK12.99
9Fructose-1,6-bisphosphatase deficiencyEnrichmentFBP12.99
10Triosephosphate isomerase deficiencyEnrichmentTPI12.99
11Retinitis pigmentosa 79EnrichmentHK12.99
12Glucose/galactose malabsorptionEnrichmentSLC5A12.99
13Neuropathy, hereditary motor and sensory, russe typeEnrichmentHK12.99
14Neurodevelopmental disorder with visual defects and brain anomaliesEnrichmentHK12.99
15Anemia, congenital, nonspherocytic hemolytic, 4EnrichmentGPI2.99
16Sengers syndromeEnrichmentTKFC2.96
17Neuromuscular diseaseEnrichmentSORD2.88
18Fanconi-bickel syndromeEnrichmentSLC2A22.69
19Congenital disorder of glycosylation, type itEnrichmentPGM12.69
20Renal glucosuriaEnrichmentSLC5A12.38
21HypoglycemiaEnrichmentG6PC12.29
22Hereditary spherocytosisEnrichmentGPI2.21
23Hemolytic anemiaEnrichmentGPI2.14
24Glycogen storage diseaseEnrichmentG6PC11.95
25Congenital long qt syndromeEnrichmentSLC2A21.91
26Congenital disorder of glycosylation, type inEnrichmentPGM11.76
27Long qt syndrome 1EnrichmentSLC2A21.52
28Type 2 diabetes mellitusEnrichmentSLC2A21.37
29Autism spectrum disorderEnrichmentHK10.97
30Retinitis pigmentosaEnrichmentHK10.70
31Hereditary retinal dystrophyEnrichmentHK10.58
32Fundus dystrophyEnrichmentHK10.58

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