RHO GTPases Activate NADPH Oxidases

No Pathway Network information available for RHO GTPases Activate NADPH Oxidases

Pathways in the RHO GTPases Activate NADPH Oxidases SuperPath

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

Disorders associated with RHO GTPases Activate NADPH Oxidases SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Chronic granulomatous diseaseEnrichmentCYBA, CYBB, NCF1, NCF2, NCF410.48
2Granulomatous disease, chronic, autosomal recessive, 2EnrichmentNCF1, NCF25.05
3Granulomatous disease, chronic, x-linkedEnrichmentCYBB, NCF14.75
4Granulomatous disease, chronic, autosomal recessive, 4EnrichmentCYBA2.75
5Immunodeficiency 34EnrichmentCYBB2.75
6Immunodeficiency 73a with defective neutrophil chemotaxis and leukocytosisEnrichmentRAC22.75
7Autoimmune lymphoproliferative syndrome, type iiiEnrichmentPRKCD2.75
8Noonan syndrome 13EnrichmentMAPK12.75
9Immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemiaEnrichmentRAC22.75
10Immunodeficiency 73b with defective neutrophil chemotaxis and lymphopeniaEnrichmentRAC22.75
11Infantile lad-like disease due to rac2 deficiencyEnrichmentRAC22.75
12Reticular dysgenesis-like severe combined immunodeficiencyEnrichmentRAC22.75
13Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndromEnrichmentRAC12.75
14Rac2-related combined immunodeficiency-bronchiectasis-cancer-predisposing syndromeEnrichmentRAC22.75
15Granulomatous disease, chronic, autosomal recessive, 1EnrichmentNCF12.45
16Granulomatous disease, chronic, autosomal recessive, 3EnrichmentNCF42.45
17Intellectual developmental disorder, autosomal dominant 48EnrichmentRAC12.45
18Autoimmune polyendocrine syndrome, type i, with or without reversible metaphyseal dysplasiaEnrichmentCYBA2.28
19Autoimmune polyendocrine syndrome type 1EnrichmentCYBA2.28
20Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK12.15
21Cardiomyopathy, familial hypertrophic, 4EnrichmentNCF11.80
22Neurodevelopmental disorder with dysmorphic facies and distal limb anomaliesEnrichmentRAC11.80
23Specific learning disabilityEnrichmentMAPK11.71
24Chromosome 1p36 deletion syndromeEnrichmentPRKCZ1.64
25Heart, malformation ofEnrichmentMAPK11.50
26Williams-beuren syndromeEnrichmentNCF11.46
27MicrocephalyEnrichmentMAPK10.71

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