D-galactose degradation V (Leloir pathway)

Pathway network for the D-galactose degradation V (Leloir pathway) SuperPath

Sources:
  • PubChem
  • WikiPathways
  • Reactome

Gene overlap in member pathways for D-galactose degradation V (Leloir pathway) SuperPath

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

Disorders associated with D-galactose degradation V (Leloir pathway) SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Glycogen storage disease ivDirect
2Glycogen storage diseaseDirect
3Galactosemia ivDirect
4Galactosemia iiDirect
5GalactosemiaDirect
6Galactosemia iiiEnrichmentGALE3.35
7Thrombocytopenia 13, syndromicEnrichmentGALE3.35
8Galactosemia iEnrichmentGALT3.05
9Congenital disorder of glycosylation, type itEnrichmentPGM13.05
10Epidermolysis bullosa, junctional 5a, intermediateEnrichmentGALK13.05
11Glycogen storage disease viEnrichmentPYGL3.02
12Polyglucosan body neuropathy, adult formEnrichmentGBE13.02
13Glucose/galactose malabsorptionEnrichmentSLC5A13.02
14Adult polyglucosan body diseaseEnrichmentGBE13.02
15Fanconi-bickel syndromeEnrichmentSLC2A22.72
16Glycogen storage disease 0, liverEnrichmentGYS22.72
17Osteogenesis imperfecta, type xvEnrichmentGBE12.72
18Glycogen storage disease xvEnrichmentGYG12.72
19Polyglucosan body myopathy 2EnrichmentGYG12.72
20Glycogen storage disease 0, muscleEnrichmentGYS12.72
21Glycogen storage disorder due to hepatic glycogen synthase deficiencyEnrichmentGYS22.72
22Glycogen storage disease due to muscle and heart glycogen synthase deficiencyEnrichmentGYS12.72
23Epidermolysis bullosa simplex 1c, localizedEnrichmentGALK12.66
24Epidermolysis bullosa, junctional 1a, intermediateEnrichmentGALK12.58
25Epidermolysis bullosa, junctional 5b, with pyloric atresiaEnrichmentGALK12.58
26Junctional epidermolysis bullosa non-herlitz typeEnrichmentGALK12.58
27Cutis laxa, autosomal recessive, type ibEnrichmentGBE12.54
28Epidermolysis bullosa simplexEnrichmentGALK12.51
29Renal glucosuriaEnrichmentSLC5A12.42
30Junctional epidermolysis bullosaEnrichmentGALK12.40
31Congenital disorder of glycosylation, type inEnrichmentPGM12.13
32Congenital long qt syndromeEnrichmentSLC2A21.94
33Primary ovarian insufficiencyEnrichmentGALT1.59
34Long qt syndrome 1EnrichmentSLC2A21.55
35Fetal akinesia deformation sequence 1EnrichmentGBE11.46
36Type 2 diabetes mellitusEnrichmentSLC2A21.40
37Distal arthrogryposisEnrichmentGBE11.40

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