Arsenic metabolism and reactive oxygen species generation

No Pathway Network information available for Arsenic metabolism and reactive oxygen species generation

Pathways in the Arsenic metabolism and reactive oxygen species generation SuperPath

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

Disorders associated with Arsenic metabolism and reactive oxygen species generation SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Pheochromocytoma/paraganglioma syndrome 5EnrichmentSDHA3.18
2Mitochondrial complex iv deficiency, nuclear type 14EnrichmentCOA33.18
3AcatalasemiaEnrichmentCAT3.18
4Cardiomyopathy, dilated, 1ggEnrichmentSDHA3.18
5Mitochondrial complex iii deficiency, nuclear type 10EnrichmentUQCRFS13.18
6Neurodegeneration with ataxia and late-onset optic atrophyEnrichmentSDHA3.18
7Polymyoclonus, infantileEnrichmentSDHA2.88
8Charcot-marie-tooth disease, axonal, type 2ddEnrichmentATP1A12.88
9Hypomagnesemia, seizures, and impaired intellectual development 2EnrichmentATP1A12.88
10Spastic tetraplegia and axial hypotonia, progressiveEnrichmentSOD12.88
11Carney triadEnrichmentSDHA2.70
12ParagangliomaEnrichmentSDHA2.70
13Brain cancerEnrichmentSDHA2.70
14Pheochromocytoma/paraganglioma syndrome 1EnrichmentSDHA2.58
15Mitochondrial complex ii deficiency, nuclear type 1EnrichmentSDHA2.58
16Propionic acidemiaEnrichmentUQCRFS12.58
17Pilocytic astrocytomaEnrichmentSDHA2.58
18Mitochondrial complex ii deficiencyEnrichmentSDHA2.58
19Amyotrophic lateral sclerosis 10 with or without frontotemporal dementiaEnrichmentSOD12.48
20Gastrointestinal stromal tumorEnrichmentSDHA2.33
21Motor neuron diseaseEnrichmentSOD12.33
22Amyotrophic lateral sclerosis 1EnrichmentSOD12.18
23Isolated complex iii deficiencyEnrichmentUQCRFS12.14
24Lactic acidosisEnrichmentUQCRFS12.10
25PheochromocytomaEnrichmentSDHA2.03
26Cox deficiency, benign infantile mitochondrial myopathyEnrichmentCOA32.03
27RhabdomyosarcomaEnrichmentSDHA1.98
28Hereditary paraganglioma-pheochromocytoma syndromesEnrichmentSDHA1.86
29Mitochondrial complex iv deficiency, nuclear type 1EnrichmentCOA31.84
30Hereditary breast carcinomaEnrichmentSDHA1.54
31Familial isolated dilated cardiomyopathyEnrichmentSDHA1.46
32Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentSOD11.42
33Leigh syndrome, nuclearEnrichmentSDHA1.35
34Breast cancerEnrichmentSDHA1.31
35Leigh diseaseEnrichmentSDHA1.31
36Inherited cancer-predisposing syndromeEnrichmentSDHA1.07

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