CD40/CD40L signaling

No Pathway Network information available for CD40/CD40L signaling

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

Disorders associated with CD40/CD40L signaling SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Common variable immunodeficiencyEnrichmentCD40LG, NFKB14.07
2Proteus syndromeEnrichmentAKT12.69
3Spinocerebellar ataxia, autosomal recessive 23EnrichmentTDP22.69
446,xy sex reversal 6EnrichmentMAP3K12.69
5Immunodeficiency with hyper-igm, type 1EnrichmentCD40LG2.69
6Immunodeficiency 132aEnrichmentTRAF32.69
7Immunodeficiency 132bEnrichmentTRAF32.69
8Immunodeficiency with hyper-igm, type 3EnrichmentCD402.69
9Cowden syndrome 6EnrichmentAKT12.69
10T-b+ severe combined immunodeficiency due to jak3 deficiencyEnrichmentJAK32.69
11Familial behcet-like autoinflammatory syndromeEnrichmentTNFAIP32.69
12Immunodeficiency 112EnrichmentMAP3K142.69
13Cd40 ligand deficiencyEnrichmentCD40LG2.69
14Nik deficiencyEnrichmentMAP3K142.69
15Burkitt lymphomaEnrichmentMYC2.38
16Ectodermal dysplasia and immunodeficiency 2EnrichmentNFKBIA2.38
17Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.38
18Autoinflammatory syndrome, familial, behcet-like 1EnrichmentTNFAIP32.38
19Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA2.38
20Autoimmune disease, multisystem, infantile-onset, 3EnrichmentCBLB2.38
21Rela fusion-positive ependymomaEnrichmentRELA2.38
22Ectodermal dysplasia and immune deficiencyEnrichmentNFKBIA2.38
23Common variable immunodeficiency 12EnrichmentNFKB12.38
24Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiencyEnrichmentJAK32.21
25Nasopharyngeal carcinomaEnrichmentNFKBIA2.21
26High-grade b-cell lymphoma double-hit/triple-hitEnrichmentMYC2.21
27Adenosine deaminase deficiencyEnrichmentJAK32.08
28Ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominantEnrichmentTRAF61.99
29Lymphoma, mucosa-associated lymphoid typeEnrichmentBIRC31.99
30Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-negativeEnrichmentJAK31.99
31Herpes simplex virus encephalitisEnrichmentTRAF31.99
32Breast cancerEnrichmentAKT1, JUN1.98
33Breast adenocarcinomaEnrichmentAKT11.91
34Ovarian cancerEnrichmentAKT1, MAP3K11.74
35Cowden syndromeEnrichmentAKT11.73
36Ciliary dyskinesia, primary, 3EnrichmentNFKB11.69
3746,xy complete gonadal dysgenesisEnrichmentMAP3K11.65
38MeningiomaEnrichmentAKT11.61
39Nk-cell enteropathyEnrichmentJAK31.58
4046,xy partial gonadal dysgenesisEnrichmentMAP3K11.54
41GliosarcomaEnrichmentNFKBIA1.49
42Giant cell glioblastomaEnrichmentNFKBIA1.46
43Multisystem inflammatory syndrome in childrenEnrichmentTRAF31.35
44Precursor t-cell acute lymphoblastic leukemiaEnrichmentMYC1.33
45Severe covid-19EnrichmentJAK31.23
46Severe combined immunodeficiencyEnrichmentJAK31.18
47Systemic lupus erythematosusEnrichmentTNFAIP31.11
48Hereditary breast carcinomaEnrichmentAKT11.06
49Colorectal cancerEnrichmentAKT10.78

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