Canonical NF-kappaB pathway

No Pathway Network information available for Canonical NF-kappaB pathway

Pathways in the Canonical NF-kappaB pathway SuperPath

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

Disorders associated with Canonical NF-kappaB pathway SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Ectodermal dysplasia and immune deficiencyEnrichmentIKBKG, NFKBIA5.52
2Lymphoma, mucosa-associated lymphoid typeEnrichmentBCL10, MALT14.52
3GliosarcomaEnrichmentATM, NFKBIA3.45
4Giant cell glioblastomaEnrichmentATM, NFKBIA3.40
5Behcet syndromeEnrichmentNOD2, TNFRSF1A3.30
6MalariaEnrichmentIKBKG, TNF3.13
7Autoinflammatory diseaseEnrichmentNOD2, TNFRSF1A3.09
8Severe combined immunodeficiencyEnrichmentIKBKB, MALT12.81
9Periodic fever, familial, autosomal dominantEnrichmentTNFRSF1A2.75
10Incontinentia pigmentiEnrichmentIKBKG2.75
11Autoinflammatory disease, systemic, x-linkedEnrichmentIKBKG2.75
12Fetal encasement syndromeEnrichmentCHUK2.75
13Blau syndromeEnrichmentNOD22.75
14Immunodeficiency 15bEnrichmentIKBKB2.75
15Immunodeficiency 15aEnrichmentIKBKB2.75
16Ectodermal dysplasia and immunodeficiency 1EnrichmentIKBKG2.75
17Multiple sclerosis 5EnrichmentTNFRSF1A2.75
18Immunodeficiency 12EnrichmentMALT12.75
19Endometrial serous adenocarcinomaEnrichmentATM2.75
20Tnf receptor-associated periodic fever syndromeEnrichmentTNFRSF1A2.75
21Bartsocas-papas syndrome 2EnrichmentCHUK2.75
22Sezary's diseaseEnrichmentBCL102.75
23Familial behcet-like autoinflammatory syndromeEnrichmentTNFAIP32.75
24B-cell non-hodgkin lymphomaEnrichmentATM2.75
25Cerebral cavernous malformations 5EnrichmentMAP3K32.75
26Combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to ikbka deficiencyEnrichmentCHUK2.75
27Distal monosomy 12pEnrichmentERC12.75
28Verrucous hemangiomaEnrichmentMAP3K32.75
29Mucosa-associated lymphomaEnrichmentBCL102.75
30Systemic lupus erythematosusEnrichmentTNF, TNFAIP32.67
31Cylindromatosis, familialEnrichmentCYLD2.45
32Trichoepithelioma, multiple familial, 1EnrichmentCYLD2.45
33Immunodeficiency 33EnrichmentIKBKG2.45
34Ectodermal dysplasia and immunodeficiency 2EnrichmentNFKBIA2.45
35Immunodeficiency 37EnrichmentBCL102.45
36Yao syndromeEnrichmentNOD22.45
37Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.45
38Autoinflammatory syndrome, familial, behcet-like 1EnrichmentTNFAIP32.45
39Cardiac valvular dysplasia, x-linkedEnrichmentATM2.45
40Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA2.45
41Frontotemporal dementia and/or amyotrophic lateral sclerosis 8EnrichmentCYLD2.45
42Brooke-spiegler syndromeEnrichmentCYLD2.45
43Immunodeficiency 127EnrichmentTNF2.45
44Rela fusion-positive ependymomaEnrichmentRELA2.45
45Macrocephaly, dysmorphic facies, and psychomotor retardationEnrichmentERC12.45
46High grade gliomaEnrichmentATM2.45
47T-cell prolymphocytic leukemiaEnrichmentATM2.45
48Glucosephosphate dehydrogenase deficiencyEnrichmentIKBKG2.45
49Intermittent hydrarthrosisEnrichmentTNFRSF1A2.45
50Crohn's diseaseEnrichmentNOD22.45
51Primary mediastinal large b-cell lymphomaEnrichmentXPO12.45
52Common variable immunodeficiency 12EnrichmentNFKB12.45
53Myeloma, multipleEnrichmentATM, CYLD2.36
54Mesothelioma, malignantEnrichmentBCL102.28
55Ataxia-telangiectasiaEnrichmentATM2.28
56Polycythemia veraEnrichmentATM2.28
57Psoriatic arthritisEnrichmentTNF2.28
58Nasopharyngeal carcinomaEnrichmentNFKBIA2.28
59Koolen-de vries syndromeEnrichmentATM2.28
60T-cell acute lymphoblastic leukemiaEnrichmentBCL102.28
61AdenocarcinomaEnrichmentATM2.28
62Migraine without auraEnrichmentTNF2.28
63Testicular cancerEnrichmentBCL102.28
64Mantle cell lymphomaEnrichmentATM2.15
65Cerebral malariaEnrichmentTNF2.15
66Oculomotor apraxiaEnrichmentATM2.15
67Ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominantEnrichmentTRAF62.05
68Anemia, congenital, nonspherocytic hemolytic, 1EnrichmentIKBKG2.05
69Follicular lymphomaEnrichmentBCL102.05
70GlioblastomaEnrichmentATM2.05
71Vascular dementiaEnrichmentTNF2.05
72Colorectal cancerEnrichmentATM, BCL101.99
73Testicular germ cell tumorEnrichmentBCL101.98
74Clear cell renal cell carcinomaEnrichmentATM1.98
75Renal cell carcinoma, papillary, 1EnrichmentATM1.91
76Common variable immunodeficiencyEnrichmentNFKB11.91
77Lymphoma, non-hodgkin, familialEnrichmentBCL101.85
78Isolated split hand-split foot malformationEnrichmentBTRC1.85
79Charge syndromeEnrichmentTNFRSF1A1.80
80Inflammatory bowel disease 1EnrichmentNOD21.80
81Coronary heart disease 5EnrichmentIKBKG1.80
82Colonic benign neoplasmEnrichmentATM1.80
83Lynch syndrome 1EnrichmentATM1.76
84Leukemia, chronic lymphocyticEnrichmentATM1.76
85Ciliary dyskinesia, primary, 3EnrichmentNFKB11.76
86Immune deficiency diseaseEnrichmentATM1.71
87AsthmaEnrichmentTNF1.71
88Combined immunodeficiencyEnrichmentMALT11.71
89Combined t cell and b cell immunodeficiencyEnrichmentMALT11.71
90Uterine corpus cancerEnrichmentATM1.71
91Familial colorectal cancer type xEnrichmentATM1.71
92Combined t and b cell immunodeficiencyEnrichmentMALT11.71
93Inherited cancer-predisposing syndromeEnrichmentATM, CYLD1.65
94Breast-ovarian cancer, familial 1EnrichmentATM1.64
95Alzheimer's diseaseEnrichmentTNF1.64
96Multiple sclerosisEnrichmentTNFRSF1A1.61
97Renal cell carcinoma, nonpapillaryEnrichmentATM1.58
98Endometrial cancerEnrichmentATM1.44
99Pancreatic cancerEnrichmentATM1.36
100Bladder cancerEnrichmentATM1.30
101Prostate cancerEnrichmentATM1.30
102Differentiated thyroid carcinomaEnrichmentERC11.30
103Gastric cancerEnrichmentATM1.13
104Hereditary breast carcinomaEnrichmentATM1.12
105Hereditary breast ovarian cancer syndromeEnrichmentATM1.03
106Breast cancerEnrichmentATM0.90
107Ovarian cancerEnrichmentATM0.78

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