Diseases of Immune System

Pathway network for the Diseases of Immune System SuperPath

Sources:
  • Reactome
  • WikiPathways
  • PubChem

Pathways in the Diseases of Immune System SuperPath

#NameSourceGenes
1Diseases of Immune SystemReactome
2Diseases associated with the TLR signaling cascadeReactome
3Toll-like receptor signaling related to MyD88WikiPathways
4Endogenous TLR signalingPubChem
5Regulation of TLR by endogenous ligandReactome
6IRAK4 deficiency (TLR2/4)Reactome
7MyD88 deficiency (TLR2/4)Reactome
8IRAK4 deficiency (TLR5)Reactome
9Transfer of LPS from LBP carrier to CD14Reactome
10MyD88 deficiency (TLR5)Reactome

Gene overlap in member pathways for Diseases of Immune System SuperPath

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

Disorders associated with Diseases of Immune System SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Immune deficiency diseaseDirect
2Herpes simplex virus encephalitisEnrichmentTBK1, TICAM1, TLR3, TRAF39.89
3Dysfibrinogenemia, congenitalEnrichmentFGA, FGB, FGG8.43
4Familial dysfibrinogenemiaEnrichmentFGA, FGB, FGG8.43
5Familial hypofibrinogenemiaEnrichmentFGA, FGB, FGG8.43
6Afibrinogenemia, congenitalEnrichmentFGA, FGB, FGG7.83
7Multisystem inflammatory syndrome in childrenEnrichmentIRF3, TLR3, TLR6, TRAF36.80
8Immunodeficiency 33EnrichmentIKBKG, IRAK45.52
9Transient predisposition to invasive pyogenic bacterial infectionEnrichmentIRAK4, MYD885.52
10Common variable immunodeficiencyEnrichmentNFKB1, NFKB23.98
11Interstitial lung disease 2EnrichmentSFTPA1, SFTPA23.47
12MalariaEnrichmentIKBKG, TIRAP3.13
13Leprosy 3EnrichmentTLR22.79
14Coronary heart disease 7EnrichmentCD362.79
15Brachyphalangy, polydactyly, and tibial aplasia/hypoplasiaEnrichmentHMGB12.79
16Leprosy 5EnrichmentTLR12.79
17Interstitial lung disease 1EnrichmentSFTPA12.79
18Immunodeficiency 74, covid19-related, x-linkedEnrichmentTLR72.79
19X-linked immunodeficiency 74EnrichmentTLR72.79
20Systemic lupus erythematosus 17EnrichmentTLR72.79
21Deafness, autosomal dominant 5EnrichmentGSDME2.79
22Platelet glycoprotein iv deficiencyEnrichmentCD362.79
23Macular degeneration, age-related, 10EnrichmentTLR42.79
24Congenital fibrinogen deficiencyEnrichmentFGG2.79
25Incontinentia pigmentiEnrichmentIKBKG2.75
26Autoinflammatory disease, systemic, x-linkedEnrichmentIKBKG2.75
27Immunodeficiency 68EnrichmentMYD882.75
28Macroglobulinemia, waldenstrom 1EnrichmentMYD882.75
29Immunodeficiency 83 viral infectionsEnrichmentTLR32.75
30Bacteremia 1EnrichmentTIRAP2.75
31Fetal encasement syndromeEnrichmentCHUK2.75
32Encephalopathy, acute, infection-induced 6EnrichmentTICAM12.75
33Immunodeficiency 15bEnrichmentIKBKB2.75
34Immunodeficiency 15aEnrichmentIKBKB2.75
35Ectodermal dysplasia and immunodeficiency 1EnrichmentIKBKG2.75
36Meester-loeys syndromeEnrichmentBGN2.75
37Spastic paraplegia 13, autosomal dominantEnrichmentHSPD12.75
38Immunodeficiency 67EnrichmentIRAK42.75
39Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomaliesEnrichmentRHOA2.75
40Bartsocas-papas syndrome 2EnrichmentCHUK2.75
41Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomaliesEnrichmentRHOA2.75
42Waldenstram macroglobulinemiaEnrichmentMYD882.75
43Combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to ikbka deficiencyEnrichmentCHUK2.75
44Legionnaire diseaseEnrichmentTLR52.64
45Immunodeficiency 39 viral infectionsEnrichmentIRF72.64
46Encephalopathy, acute, infection-induced 7EnrichmentIRF32.64
47Noonan syndrome 13EnrichmentMAPK12.64
48Immunodeficiency 92EnrichmentREL2.64
49Systemic lupus erythematosus 1EnrichmentTLR52.64
50Immunodeficiency 132aEnrichmentTRAF32.64
51Immunodeficiency 132bEnrichmentTRAF32.64
52Immunodeficiency 39EnrichmentIRF72.64
53MelioidosisEnrichmentTLR52.64
54Autoinflammation with arthritis and vasculitisEnrichmentTBK12.64
55Corticobasal syndromeEnrichmentTBK12.64
56Deficiency in anterior pituitary function - variable immunodeficiency syndromeEnrichmentNFKB22.64
57Immunodeficiency 53EnrichmentRELB2.64
58Encephalopathy, acute, infection-induced 8EnrichmentTBK12.64
59Hypobetalipoproteinemia, familial, 1EnrichmentAPOB2.49
60Leprosy 1EnrichmentTLR62.49
61HypobetalipoproteinemiaEnrichmentAPOB2.49
62Wagner vitreoretinopathyEnrichmentVCAN2.45
63Spondyloepimetaphyseal dysplasia, x-linkedEnrichmentBGN2.45
64Leukodystrophy, hypomyelinating, 4EnrichmentHSPD12.45
65Congenital dyserythropoietic anemiaEnrichmentIRAK42.45
66Ectodermal dysplasia and immune deficiencyEnrichmentIKBKG2.45
67Glucosephosphate dehydrogenase deficiencyEnrichmentIKBKG2.45
68Wagner diseaseEnrichmentVCAN2.45
69Systemic lupus erythematosusEnrichmentIRAK1, TLR72.45
70Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.34
71Immunodeficiency, common variable, 10EnrichmentNFKB22.34
72Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA2.34
73Rela fusion-positive ependymomaEnrichmentRELA2.34
74Frontotemporal dementia and/or amyotrophic lateral sclerosis 4EnrichmentTBK12.34
75Common variable immunodeficiency 12EnrichmentNFKB12.34
76Hypercholesterolemia, familial, 2EnrichmentAPOB2.31
77Blood platelet diseaseEnrichmentCD362.19
78Cerebral malariaEnrichmentCD362.19
79Immunodeficiency 98 with autoinflammation, x-linkedEnrichmentTLR82.16
80Pediatric systemic lupus erythematosusEnrichmentIRAK12.15
81Hyperlipidemia, familial combined, 3EnrichmentAPOB2.09
82Amyloidosis, hereditary systemic 2EnrichmentFGA2.09
83Anemia, congenital, nonspherocytic hemolytic, 1EnrichmentIKBKG2.05
84Anemia, autoimmune hemolyticEnrichmentTLR82.04
85Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK12.04
86Immunodeficiency, common variable, 1EnrichmentNFKB22.04
87Hemihyperplasia, isolatedEnrichmentRHOA1.98
88Thrombophilia due to thrombin defectEnrichmentFGA1.95
89Ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominantEnrichmentTRAF61.94
90Spastic paraplegia 4, autosomal dominantEnrichmentFGG1.89
91Homozygous familial hypercholesterolemiaEnrichmentAPOB1.89
92Rheumatoid arthritisEnrichmentTLR11.84
93Coronary heart disease 5EnrichmentAPOB1.84
94Motor neuron diseaseEnrichmentTBK11.80
95Stickler syndromeEnrichmentVCAN1.76
96Progressive non-fluent aphasiaEnrichmentTBK11.69
97Hypercholesterolemia, familial, 1EnrichmentAPOB1.68
98Frontotemporal dementia and/or amyotrophic lateral sclerosis 1EnrichmentTBK11.65
99Ciliary dyskinesia, primary, 3EnrichmentNFKB11.65
100Familial hypercholesterolemiaEnrichmentAPOB1.62
101Specific learning disabilityEnrichmentMAPK11.60
102Behcet syndromeEnrichmentTLR41.52
103Human immunodeficiency virus type 1EnrichmentTLR31.50
104Diffuse large b-cell lymphomaEnrichmentMYD881.48
105LeukodystrophyEnrichmentHSPD11.46
106Heart, malformation ofEnrichmentMAPK11.39
107Severe combined immunodeficiencyEnrichmentIKBKB1.25
108Familial thoracic aortic aneurysm and aortic dissectionEnrichmentBGN1.12
109ThrombocytopeniaEnrichmentFGG1.12
110Rare autosomal dominant non-syndromic sensorineural deafness type dfnaEnrichmentGSDME1.09
111Rare genetic deafnessEnrichmentGSDME0.92
112Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentTBK10.90
113Colorectal cancerEnrichmentTLR20.88
114MicrocephalyEnrichmentMAPK10.61
115Hereditary retinal dystrophyEnrichmentVCAN0.39
116Fundus dystrophyEnrichmentVCAN0.39

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