Detoxification of Reactive Oxygen Species

Pathway network for the Detoxification of Reactive Oxygen Species SuperPath

Sources:
  • Reactome
  • PubChem
  • PharmGKB

Gene overlap in member pathways for Detoxification of Reactive Oxygen Species SuperPath

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

Disorders associated with Detoxification of Reactive Oxygen Species SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Chronic granulomatous diseaseEnrichmentCYBA, CYBB, NCF1, NCF2, NCF410.49
2Granulomatous disease, chronic, autosomal recessive, 2EnrichmentNCF1, NCF24.69
3Granulomatous disease, chronic, x-linkedEnrichmentCYBB, NCF14.39
4Microvascular complications of diabetes 6EnrichmentSOD23.29
5AcatalasemiaEnrichmentCAT3.29
6Glutathione peroxidase deficiencyEnrichmentGPX13.29
7Anemia, congenital, nonspherocytic hemolytic, 10EnrichmentGSR3.29
8Spastic tetraplegia and axial hypotonia, progressiveEnrichmentSOD12.99
9Amyotrophic lateral sclerosis 10 with or without frontotemporal dementiaEnrichmentSOD12.59
10Cole-carpenter syndrome 1EnrichmentP4HB2.58
11Granulomatous disease, chronic, autosomal recessive, 4EnrichmentCYBA2.58
12Neuronopathy, distal hereditary motor, x-linkedEnrichmentATP7A2.58
13Immunodeficiency 34EnrichmentCYBB2.58
14Spinocerebellar ataxia, autosomal recessive 32EnrichmentPRDX32.58
15Combined oxidative phosphorylation deficiency 29EnrichmentTXN22.58
16Occipital horn syndromeEnrichmentATP7A2.58
17Glucocorticoid deficiency 5EnrichmentTXNRD22.58
18Corneal dystrophy, punctiform and polychromatic pre-descemetEnrichmentPRDX32.58
19Intellectual developmental disorder with or without peripheral neuropathyEnrichmentNUDT22.58
20Motor neuron diseaseEnrichmentSOD12.44
21Amyotrophic lateral sclerosis 1EnrichmentSOD12.29
22Granulomatous disease, chronic, autosomal recessive, 1EnrichmentNCF12.28
23Granulomatous disease, chronic, autosomal recessive, 3EnrichmentNCF42.28
24Albinism, oculocutaneous, type iaEnrichmentNOX42.28
25Kala-azar 2EnrichmentGSTP12.28
26Autoimmune polyendocrine syndrome, type i, with or without reversible metaphyseal dysplasiaEnrichmentCYBA2.10
27Menkes diseaseEnrichmentATP7A2.10
28Autoimmune polyendocrine syndrome type 1EnrichmentCYBA2.10
29Cole-carpenter syndromeEnrichmentP4HB2.10
30Autosomal recessive cerebellar ataxiaEnrichmentPRDX31.88
31Familial glucocorticoid deficiencyEnrichmentTXNRD21.88
32Osteogenesis imperfecta, type iEnrichmentP4HB1.80
33Methylmalonic aciduria and homocystinuria, cblc typeEnrichmentPRDX11.68
34Cardiomyopathy, familial hypertrophic, 4EnrichmentNCF11.63
35Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentSOD11.53
36Williams-beuren syndromeEnrichmentNCF11.29
37Hirschsprung disease 1EnrichmentATP7A1.13
38Familial isolated dilated cardiomyopathyEnrichmentTXNRD20.88

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