NF-kB (NFkB) Pathway

No Pathway Network information available for NF-kB (NFkB) Pathway

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

Disorders associated with NF-kB (NFkB) Pathway SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Severe combined immunodeficiencyEnrichmentIKBKB, LCK, MALT1, ZAP705.04
2Transient predisposition to invasive pyogenic bacterial infectionEnrichmentIRAK4, MYD884.79
3Herpes simplex virus encephalitisEnrichmentTBK1, TRAF33.80
4Immune deficiency diseaseEnrichmentRIPK1, SYK3.06
5Combined immunodeficiencyEnrichmentMALT1, ZAP703.06
6Combined t cell and b cell immunodeficiencyEnrichmentMALT1, ZAP703.06
7Combined t and b cell immunodeficiencyEnrichmentMALT1, ZAP703.06
8Behcet syndromeEnrichmentTLR4, TNFRSF1A2.58
9Diffuse large b-cell lymphomaEnrichmentBTK, MYD882.58
10Tooth agenesisEnrichmentIRF6, SUMO12.45
11Periodic fever, familial, autosomal dominantEnrichmentTNFRSF1A2.39
12Cardiospondylocarpofacial syndromeEnrichmentMAP3K72.39
13Immunodeficiency 68EnrichmentMYD882.39
14Orofacial cleft 6EnrichmentIRF62.39
15Macroglobulinemia, waldenstrom 1EnrichmentMYD882.39
16Popliteal pterygium syndromeEnrichmentIRF62.39
17Frontometaphyseal dysplasia 2EnrichmentMAP3K72.39
18Immunodeficiency 15bEnrichmentIKBKB2.39
19Noonan syndrome 13EnrichmentMAPK12.39
20Immunodeficiency 82 with systemic inflammationEnrichmentSYK2.39
21Immunodeficiency 15aEnrichmentIKBKB2.39
22Immunodeficiency 48EnrichmentZAP702.39
23Orofacial cleft 10EnrichmentSUMO12.39
24Okt4 epitope deficiencyEnrichmentCD42.39
25Type 1 diabetes mellitus 5EnrichmentSUMO42.39
26Immunodeficiency 132aEnrichmentTRAF32.39
27Isolated growth hormone deficiency type iiiEnrichmentBTK2.39
28Immunodeficiency 132bEnrichmentTRAF32.39
29Immunodeficiency 67EnrichmentIRAK42.39
30Multiple sclerosis 5EnrichmentTNFRSF1A2.39
31Immunodeficiency 90 with encephalopathy, functional hyposplenia, and hepatic dysfunctionEnrichmentFADD2.39
32Immunodeficiency 12EnrichmentMALT12.39
33Macular degeneration, age-related, 10EnrichmentTLR42.39
34Autoinflammation with arthritis and vasculitisEnrichmentTBK12.39
35Autoimmune disease, multisystem, infantile-onset, 2EnrichmentZAP702.39
36Immunodeficiency 22EnrichmentLCK2.39
37Tnf receptor-associated periodic fever syndromeEnrichmentTNFRSF1A2.39
38Irf6-related disordersEnrichmentIRF62.39
39Autosomal dominant popliteal pterygium syndromeEnrichmentIRF62.39
40Corticobasal syndromeEnrichmentTBK12.39
41Autoinflammatory disease, systemic, with vasculitisEnrichmentLYN2.39
42Immunodeficiency 79EnrichmentCD42.39
43Autoinflammation with episodic fever and lymphadenopathyEnrichmentRIPK12.39
44Encephalopathy, acute, infection-induced 8EnrichmentTBK12.39
45ColitisEnrichmentSYK2.39
46Immunodeficiency 112EnrichmentMAP3K142.39
47Cerebral cavernous malformations 5EnrichmentMAP3K32.39
48Waldenstram macroglobulinemiaEnrichmentMYD882.39
49Verrucous hemangiomaEnrichmentMAP3K32.39
50Nik deficiencyEnrichmentMAP3K142.39
51Zap70-related severe combined immunodeficiencyEnrichmentZAP702.39
52Scoliosis, isolated 1EnrichmentMAPK72.09
53Immunodeficiency 33EnrichmentIRAK42.09
54Isolated growth hormone deficiency, type iii, with agammaglobulinemiaEnrichmentBTK2.09
55Ectodermal dysplasia and immunodeficiency 2EnrichmentNFKBIA2.09
56Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.09
57Agammaglobulinemia, x-linkedEnrichmentBTK2.09
58Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA2.09
59Immunodeficiency 127EnrichmentTNF2.09
60Rela fusion-positive ependymomaEnrichmentRELA2.09
61Frontotemporal dementia and/or amyotrophic lateral sclerosis 4EnrichmentTBK12.09
62Congenital dyserythropoietic anemiaEnrichmentIRAK42.09
63Ectodermal dysplasia and immune deficiencyEnrichmentNFKBIA2.09
64Immunodeficiency 57 with autoinflammationEnrichmentRIPK12.09
65Intermittent hydrarthrosisEnrichmentTNFRSF1A2.09
66ArthritisEnrichmentSYK2.09
67Van der woude syndromeEnrichmentIRF62.09
68Common variable immunodeficiency 12EnrichmentNFKB12.09
69Oculootodental syndromeEnrichmentFADD2.09
70Van der woude syndrome 1EnrichmentIRF61.92
71Agammaglobulinemia 1, autosomal recessiveEnrichmentBTK1.92
72Psoriatic arthritisEnrichmentTNF1.92
73Nasopharyngeal carcinomaEnrichmentNFKBIA1.92
74Agammaglobulinemia 1EnrichmentBTK1.92
75Frontometaphyseal dysplasiaEnrichmentMAP3K71.92
76Migraine without auraEnrichmentTNF1.92
77Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK11.79
78Cerebral malariaEnrichmentTNF1.79
79Cleft lip and alveolusEnrichmentIRF61.79
80Lymphoma, mucosa-associated lymphoid typeEnrichmentMALT11.70
81Vascular dementiaEnrichmentTNF1.70
82Cleft upper lipEnrichmentIRF61.70
83Inflammatory bowel disease 25, autosomal recessiveEnrichmentRIPK11.62
84Il10-related early-onset inflammatory bowel diseaseEnrichmentRIPK11.62
85Motor neuron diseaseEnrichmentTBK11.55
86Common variable immunodeficiencyEnrichmentNFKB11.55
87Charge syndromeEnrichmentTNFRSF1A1.44
88Progressive non-fluent aphasiaEnrichmentTBK11.44
89Frontotemporal dementia and/or amyotrophic lateral sclerosis 1EnrichmentTBK11.40
90Ciliary dyskinesia, primary, 3EnrichmentNFKB11.40
91AsthmaEnrichmentTNF1.36
92Specific learning disabilityEnrichmentMAPK11.36
93Alzheimer's diseaseEnrichmentTNF1.29
94Nk-cell enteropathyEnrichmentPIK3CB1.29
95Multiple sclerosisEnrichmentTNFRSF1A1.26
96Cleft lip/palateEnrichmentIRF61.26
97GliosarcomaEnrichmentNFKBIA1.20
98Cleft palate, isolatedEnrichmentIRF61.18
99Giant cell glioblastomaEnrichmentNFKBIA1.18
100Heart, malformation ofEnrichmentMAPK11.15
101Multisystem inflammatory syndrome in childrenEnrichmentTRAF31.07
102MalariaEnrichmentTNF1.05
103Autoinflammatory diseaseEnrichmentTNFRSF1A1.03
104Lung cancerEnrichmentMAP3K80.91
105Systemic lupus erythematosusEnrichmentTNF0.83
106Hereditary breast ovarian cancer syndromeEnrichmentRIPK10.70
107Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentTBK10.68
108MicrocephalyEnrichmentMAPK10.40

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