Oxidative stress response

No Pathway Network information available for Oxidative stress response

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

Disorders associated with Oxidative stress response SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Pulmonary disease, chronic obstructiveEnrichmentHMOX1, MGST13.38
2Immunodeficiency 34EnrichmentCYBB2.63
3Microvascular complications of diabetes 6EnrichmentSOD22.63
4Anemia, congenital, nonspherocytic hemolytic, 7EnrichmentGCLC2.63
5Anemia, congenital, nonspherocytic hemolytic, 10EnrichmentGSR2.63
6Combined oxidative phosphorylation deficiency 29EnrichmentTXN22.63
7Immunodeficiency, developmental delay, and hypohomocysteinemiaEnrichmentNFE2L22.63
8Brunner syndromeEnrichmentMAOA2.63
9Marshall-smith syndromeEnrichmentNFIX2.63
10Glucocorticoid deficiency 5EnrichmentTXNRD22.63
11AcatalasemiaEnrichmentCAT2.63
12Glutathione peroxidase deficiencyEnrichmentGPX12.63
13Malan syndromeEnrichmentNFIX2.63
14Heme oxygenase 1 deficiencyEnrichmentHMOX12.63
1519p13.3 microduplication syndromeEnrichmentNFIX2.63
16Sotos syndrome 2EnrichmentNFIX2.63
17Cystic fibrosisEnrichmentGCLC, HMOX12.59
18Xanthinuria, type iEnrichmentXDH2.33
19Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.33
20Albinism, oculocutaneous, type iaEnrichmentNOX42.33
21Spastic tetraplegia and axial hypotonia, progressiveEnrichmentSOD12.33
22Common variable immunodeficiency 12EnrichmentNFKB12.33
23LaryngomalaciaEnrichmentNFIX2.15
24MegalocorneaEnrichmentNFIX2.15
25Xanthinuria, type iiEnrichmentXDH2.15
26Granulomatous disease, chronic, x-linkedEnrichmentCYBB2.03
27Congenital generalized lipodystrophyEnrichmentFOS2.03
28Megalencephalic leukoencephalopathy with subcortical cysts 1EnrichmentGSTT21.93
29Amyotrophic lateral sclerosis 10 with or without frontotemporal dementiaEnrichmentSOD11.93
30Histiocytoid hemangiomaEnrichmentFOS1.93
31Familial glucocorticoid deficiencyEnrichmentTXNRD21.93
32Motor neuron diseaseEnrichmentSOD11.79
33Common variable immunodeficiencyEnrichmentNFKB11.79
34Lennox-gastaut syndromeEnrichmentMAPK101.73
35Chronic granulomatous diseaseEnrichmentCYBB1.68
36Amyotrophic lateral sclerosis 1EnrichmentSOD11.63
37Crigler-najjar syndrome, type iEnrichmentUGT1A61.63
38Hyperbilirubinemia, transient familial neonatalEnrichmentUGT1A61.63
39Bilirubin, serum level of, quantitative trait locus 1EnrichmentUGT1A61.63
40Ciliary dyskinesia, primary, 3EnrichmentNFKB11.63
41Crigler-najjar syndrome, type iiEnrichmentUGT1A61.63
42Gilbert syndromeEnrichmentUGT1A61.59
43Bilirubin metabolic disorderEnrichmentUGT1A61.59
44Myocardial infarctionEnrichmentGCLC1.30
45StrabismusEnrichmentNFIX1.21
46Lung cancerEnrichmentNFE2L21.14
47Familial isolated dilated cardiomyopathyEnrichmentTXNRD20.93
48Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentSOD10.89
49Colorectal cancerEnrichmentNFE2L20.73

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