SARS-CoV-2 innate immunity evasion and cell-specific immune response

No Pathway Network information available for SARS-CoV-2 innate immunity evasion and cell-specific immune response

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

Disorders associated with SARS-CoV-2 innate immunity evasion and cell-specific immune response SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Human immunodeficiency virus type 1EnrichmentCCL2, CCL3, CCL5, IL106.32
2Il10-related early-onset inflammatory bowel diseaseEnrichmentIL10, RIPK1, TGFB16.03
3Multisystem inflammatory syndrome in childrenEnrichmentIFNB1, IRF3, TRAF34.16
4Herpes simplex virus encephalitisEnrichmentTBK1, TRAF33.88
5Inflammatory bowel disease 25, autosomal recessiveEnrichmentRIPK1, TGFB13.70
6Systemic lupus erythematosusEnrichmentIL10, TLR7, TNF3.41
7Caspase 8 deficiencyEnrichmentCASP82.43
8Immunodeficiency 39 viral infectionsEnrichmentIRF72.43
9Encephalopathy, acute, infection-induced 7EnrichmentIRF32.43
10Pseudo-torch syndrome 3EnrichmentSTAT22.43
11Immunodeficiency 74, covid19-related, x-linkedEnrichmentTLR72.43
12Graft-versus-host diseaseEnrichmentIL102.43
13X-linked immunodeficiency 74EnrichmentTLR72.43
14Immunodeficiency 132aEnrichmentTRAF32.43
15Immunodeficiency 132bEnrichmentTRAF32.43
16Systemic lupus erythematosus 17EnrichmentTLR72.43
17Immunodeficiency 39EnrichmentIRF72.43
18Immunodeficiency 90 with encephalopathy, functional hyposplenia, and hepatic dysfunctionEnrichmentFADD2.43
19Autoinflammation with arthritis and vasculitisEnrichmentTBK12.43
20Singleton-merten syndrome 2EnrichmentRIGI2.43
21T-cell lymphoma, subcutaneous panniculitis-likeEnrichmentHAVCR22.43
22Corticobasal syndromeEnrichmentTBK12.43
23Autoinflammation with episodic fever and lymphadenopathyEnrichmentRIPK12.43
24Encephalopathy, acute, infection-induced 8EnrichmentTBK12.43
25Whim syndrome 2EnrichmentCXCR22.43
26Autosomal recessive severe congenital neutropenia due to cxcr2 deficiencyEnrichmentCXCR22.43
27Camurati-engelmann disease 1EnrichmentTGFB12.13
28Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.13
29Loeys-dietz syndrome 3EnrichmentSMAD32.13
30Menke-hennekam syndrome 2EnrichmentEP3002.13
31Inflammatory bowel disease, immunodeficiency, and encephalopathyEnrichmentTGFB12.13
32Immunodeficiency 127EnrichmentTNF2.13
33Frontotemporal dementia and/or amyotrophic lateral sclerosis 4EnrichmentTBK12.13
34Camurati-engelmann diseaseEnrichmentTGFB12.13
35Immunodeficiency 57 with autoinflammationEnrichmentRIPK12.13
36EsotropiaEnrichmentTFAP2A2.13
37Singleton-merten syndromeEnrichmentRIGI2.13
38Common variable immunodeficiency 12EnrichmentNFKB12.13
39Lens subluxationEnrichmentTFAP2A2.13
40Oculootodental syndromeEnrichmentFADD2.13
41Psoriatic arthritisEnrichmentTNF1.96
42Migraine without auraEnrichmentTNF1.96
43Immunodeficiency 44EnrichmentSTAT21.96
44Branchiooculofacial syndromeEnrichmentTFAP2A1.83
45Aortic aneurysmEnrichmentSMAD31.83
46Cerebral malariaEnrichmentTNF1.83
47Ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominantEnrichmentTRAF61.74
48Rubinstein-taybi syndrome 2EnrichmentEP3001.74
49AmblyopiaEnrichmentTFAP2A1.74
50Vascular dementiaEnrichmentTNF1.74
51Branchiootorenal syndrome 1EnrichmentTFAP2A1.66
52Rubinstein-taybi syndrome 1EnrichmentEP3001.66
53Chromosome 16p13.3 deletion syndrome, proximalEnrichmentEP3001.66
54Branchiootorenal syndromeEnrichmentTFAP2A1.59
55Motor neuron diseaseEnrichmentTBK11.59
56Common variable immunodeficiencyEnrichmentNFKB11.59
57Rheumatoid arthritisEnrichmentIL101.49
58Charge syndromeEnrichmentEP3001.49
59Loeys-dietz syndromeEnrichmentSMAD31.49
60Adult hepatocellular carcinomaEnrichmentCASP81.49
61Progressive non-fluent aphasiaEnrichmentTBK11.49
62Familial thoracic aortic aneurysm and dissectionEnrichmentSMAD31.49
63Cat eye syndromeEnrichmentTFAP2A1.44
64Frontotemporal dementia and/or amyotrophic lateral sclerosis 1EnrichmentTBK11.44
65Ciliary dyskinesia, primary, 3EnrichmentNFKB11.44
66Immune deficiency diseaseEnrichmentRIPK11.40
67AsthmaEnrichmentTNF1.40
68EpicanthusEnrichmentTFAP2A1.36
69Alzheimer's diseaseEnrichmentTNF1.33
70Aortic aneurysm, familial thoracic 1EnrichmentSMAD31.30
71Polydactyly, postaxial, type a1EnrichmentEP3001.27
72Rare genetic intellectual disabilityEnrichmentEP3001.27
73Behcet syndromeEnrichmentIL101.17
74Ehlers-danlos syndromeEnrichmentSMAD31.17
75Hepatocellular carcinomaEnrichmentCASP81.11
76MicrophthalmiaEnrichmentTFAP2A1.11
77MalariaEnrichmentTNF1.09
78Hirschsprung disease 1EnrichmentNUP980.99
79Lung cancerEnrichmentCASP80.95
80Cystic fibrosisEnrichmentTGFB10.95
81Connective tissue diseaseEnrichmentSMAD30.95
82Familial thoracic aortic aneurysm and aortic dissectionEnrichmentSMAD30.82
83HypertelorismEnrichmentTFAP2A0.76
84Hereditary breast ovarian cancer syndromeEnrichmentRIPK10.73
85Myeloma, multipleEnrichmentTRAF50.73
86Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentTBK10.71
87Breast cancerEnrichmentCASP80.62
88Colorectal cancerEnrichmentEP3000.56
89MicrocephalyEnrichmentEP3000.44

Loading...
Loading...
Loading...