Photodynamic therapy-induced NF-kB survival signaling

No Pathway Network information available for Photodynamic therapy-induced NF-kB survival signaling

Pathways in the Photodynamic therapy-induced NF-kB survival signaling SuperPath

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

Disorders associated with Photodynamic therapy-induced NF-kB survival signaling SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Common variable immunodeficiencyEnrichmentCD40LG, NFKB1, NFKB26.26
2MalariaEnrichmentICAM1, NOS2, TNF4.87
3Cerebral malariaEnrichmentICAM1, TNF4.61
4Systemic-onset juvenile idiopathic arthritisEnrichmentIL6, MIF4.61
5Rheumatoid arthritis, systemic juvenileEnrichmentIL6, MIF4.39
6Glucocorticoid resistance, generalizedEnrichmentNR3C12.69
7Fetal encasement syndromeEnrichmentCHUK2.69
8Immunodeficiency 15bEnrichmentIKBKB2.69
9Immunodeficiency 69EnrichmentIFNG2.69
10Noonan syndrome 13EnrichmentMAPK12.69
11Immunodeficiency 15aEnrichmentIKBKB2.69
12Immunodeficiency 92EnrichmentREL2.69
13Deficiency in anterior pituitary function - variable immunodeficiency syndromeEnrichmentNFKB22.69
14Immunodeficiency 53EnrichmentRELB2.69
15Bartsocas-papas syndrome 2EnrichmentCHUK2.69
16Combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to ikbka deficiencyEnrichmentCHUK2.69
17Periodic fever, familial, autosomal dominantEnrichmentTNFRSF1A2.59
18Immunodeficiency with hyper-igm, type 1EnrichmentCD40LG2.59
19Microvascular complications of diabetes 1EnrichmentVEGFA2.59
20Coronary heart disease 6EnrichmentMMP32.59
21Multiple sclerosis 5EnrichmentTNFRSF1A2.59
22Tnf receptor-associated periodic fever syndromeEnrichmentTNFRSF1A2.59
23Cd40 ligand deficiencyEnrichmentCD40LG2.59
24Systemic lupus erythematosusEnrichmentETS1, TNF2.54
25Galactosemia iiEnrichmentNR3C12.38
26Ectodermal dysplasia and immunodeficiency 2EnrichmentNFKBIA2.38
27Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.38
28Immunodeficiency, common variable, 10EnrichmentNFKB22.38
29Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA2.38
30Immunodeficiency 127EnrichmentTNF2.38
31Rela fusion-positive ependymomaEnrichmentRELA2.38
32Recessive dystrophic epidermolysis bullosaEnrichmentMMP12.38
33Ectodermal dysplasia and immune deficiencyEnrichmentNFKBIA2.38
34Common variable immunodeficiency 12EnrichmentNFKB12.38
35Metaphyseal anadysplasia 2EnrichmentMMP92.29
36Metaphyseal anadysplasiaEnrichmentMMP92.29
37Intermittent hydrarthrosisEnrichmentTNFRSF1A2.29
38Jacobsen syndromeEnrichmentETS12.21
39Tuberous sclerosis 1EnrichmentIFNG2.21
40Psoriatic arthritisEnrichmentTNF2.21
41Hepatitis c virusEnrichmentIFNG2.21
42Nasopharyngeal carcinomaEnrichmentNFKBIA2.21
43Tuberous sclerosis 2EnrichmentIFNG2.21
44Migraine without auraEnrichmentTNF2.21
45Multicentric osteolysis, nodulosis, and arthropathyEnrichmentMMP22.11
46Kaposi sarcomaEnrichmentIL62.08
47Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK12.08
48Immunodeficiency, common variable, 1EnrichmentNFKB22.08
49Congenital generalized lipodystrophyEnrichmentFOS2.08
50Histiocytoid hemangiomaEnrichmentFOS1.99
51Vascular dementiaEnrichmentTNF1.99
52Idiopathic aplastic anemiaEnrichmentIFNG1.99
53Mantle cell lymphomaEnrichmentCCND11.99
54Breast cancerEnrichmentIL2, JUN1.98
55Type 1 diabetes mellitusEnrichmentIL61.91
56Ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominantEnrichmentTRAF61.89
57Lymphoma, mucosa-associated lymphoid typeEnrichmentBIRC31.89
58Von hippel-lindau syndromeEnrichmentCCND11.89
59Inflammatory bowel disease 1EnrichmentIL61.73
60Primary hyperaldosteronismEnrichmentNR3C11.73
61Ciliary dyskinesia, primary, 3EnrichmentNFKB11.69
62Aplastic anemiaEnrichmentIFNG1.69
63AsthmaEnrichmentTNF1.65
64Specific learning disabilityEnrichmentMAPK11.65
65Charge syndromeEnrichmentTNFRSF1A1.64
66Leukemia, chronic lymphocyticEnrichmentCCND11.59
67Alzheimer's diseaseEnrichmentTNF1.58
68GliosarcomaEnrichmentNFKBIA1.49
69Giant cell glioblastomaEnrichmentNFKBIA1.46
70Multiple sclerosisEnrichmentTNFRSF1A1.45
71Heart, malformation ofEnrichmentMAPK11.44
72Human immunodeficiency virus type 1EnrichmentIFNG1.44
73Arteriovenous malformations of the brainEnrichmentIL61.41
74Behcet syndromeEnrichmentTNFRSF1A1.32
75Autoinflammatory diseaseEnrichmentTNFRSF1A1.22
76Cystic fibrosisEnrichmentMIF1.19
77Severe combined immunodeficiencyEnrichmentIKBKB1.18
78Type 2 diabetes mellitusEnrichmentIL61.08
79Gastric cancerEnrichmentIL1B0.98
80Myeloma, multipleEnrichmentCCND10.87
81Colorectal cancerEnrichmentCCND10.69
82MicrocephalyEnrichmentMAPK10.65

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