Inflammatory response pathway

No Pathway Network information available for Inflammatory response pathway

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

Disorders associated with Inflammatory response pathway SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Multiple sclerosisEnrichmentLAMA5, LAMB1, TNFRSF1A5.33
2Ehlers-danlos syndrome, arthrochalasia type, 2EnrichmentCOL1A1, COL1A25.24
3Ehlers-danlos/osteogenesis imperfecta syndromeEnrichmentCOL1A1, COL1A25.24
4Ehlers-danlos syndromeEnrichmentCOL1A1, COL1A2, COL3A14.91
5Mycosis fungoidesEnrichmentCD28, TNFRSF1B4.76
6High bone mass osteogenesis imperfectaEnrichmentCOL1A1, COL1A24.76
7Saczary syndromeEnrichmentCD28, TNFRSF1B4.76
8Ehlers-danlos syndrome, arthrochalasia type, 1EnrichmentCOL1A1, COL1A24.46
9Osteogenesis imperfecta with normal sclerae, dominant formEnrichmentCOL1A1, COL1A24.46
10Ehlers-danlos syndrome, classic type, 1EnrichmentCOL1A1, COL1A24.07
11Osteogenesis imperfecta, type iEnrichmentCOL1A1, COL1A24.07
12Classic ehlers-danlos syndromeEnrichmentCOL1A1, COL1A24.07
13Osteogenesis imperfecta, type iiEnrichmentCOL1A1, COL1A23.92
14Oligoarticular juvenile idiopathic arthritisEnrichmentIL2RA, IL2RB3.92
15Rheumatoid factor-negative juvenile idiopathic arthritisEnrichmentIL2RA, IL2RB3.92
16Nephrotic syndromeEnrichmentFN1, LAMA5, LAMB23.82
17Primary bone dysplasiaEnrichmentCOL1A1, COL1A23.59
18Combined immunodeficiencyEnrichmentIL2RG, ZAP703.51
19OsteochondrodysplasiaEnrichmentCOL1A1, COL1A23.51
20Combined t cell and b cell immunodeficiencyEnrichmentIL2RG, ZAP703.51
21Combined t and b cell immunodeficiencyEnrichmentIL2RG, ZAP703.51
22Osteogenesis imperfecta, type ivEnrichmentCOL1A1, COL1A23.36
23OsteoporosisEnrichmentCOL1A1, COL1A23.29
24Osteogenesis imperfecta, type iiiEnrichmentCOL1A1, COL1A23.23
25Brittle bone disorderEnrichmentCOL1A1, COL1A22.85
26Periodic fever, familial, autosomal dominantEnrichmentTNFRSF1A2.61
27Ehlers-danlos syndrome, cardiac valvular typeEnrichmentCOL1A22.61
28Type 1 diabetes mellitus 10EnrichmentIL2RA2.61
29Lissencephaly 5EnrichmentLAMB12.61
30Acrogeria, gottron typeEnrichmentCOL3A12.61
31Immunodeficiency 69EnrichmentIFNG2.61
32Nephrotic syndrome, type 26EnrichmentLAMA52.61
33Immunodeficiency with hyper-igm, type 1EnrichmentCD40LG2.61
34Immunodeficiency 63 with lymphoproliferation and autoimmunityEnrichmentIL2RB2.61
35Immunodeficiency 48EnrichmentZAP702.61
36Combined osteogenesis imperfecta and ehlers-danlos syndrome 2EnrichmentCOL1A22.61
37Immunodeficiency with hyper-igm, type 3EnrichmentCD402.61
38Multiple sclerosis 5EnrichmentTNFRSF1A2.61
39Immunodeficiency 123 with hpv-related verrucosisEnrichmentCD282.61
40Autoimmune disease, multisystem, infantile-onset, 2EnrichmentZAP702.61
41Immunodeficiency 22EnrichmentLCK2.61
42Tnf receptor-associated periodic fever syndromeEnrichmentTNFRSF1A2.61
43Bent bone dysplasia syndrome 2EnrichmentLAMA52.61
44Asphyxia neonatorumEnrichmentCOL1A12.61
45Cd40 ligand deficiencyEnrichmentCD40LG2.61
46Abdominal aortic aneurysmEnrichmentCOL3A12.61
47Lama5-related multisystemic syndromeEnrichmentLAMA52.61
48Zap70-related severe combined immunodeficiencyEnrichmentZAP702.61
49Severe combined immunodeficiencyEnrichmentLCK, ZAP702.54
50Ehlers-danlos syndrome, vascular typeEnrichmentCOL3A12.31
51Epiphyseal dysplasia, multiple, 1EnrichmentCOL1A12.31
52Ehlers-danlos syndrome, hypermobility typeEnrichmentCOL3A12.31
53Spondyloepimetaphyseal dysplasia, strudwick typeEnrichmentFN12.31
54Spondylometaphyseal dysplasia, corner fracture typeEnrichmentFN12.31
55Bruck syndrome 1EnrichmentCOL1A22.31
56Myasthenic syndrome, congenital, 5EnrichmentLAMB22.31
57Dermatofibrosarcoma protuberansEnrichmentCOL1A12.31
58Immunodeficiency 41 with lymphoproliferation and autoimmunityEnrichmentIL2RA2.31
59Lissencephaly 1EnrichmentLAMB12.31
60Pierson syndromeEnrichmentLAMB22.31
61Combined osteogenesis imperfecta and ehlers-danlos syndrome 1EnrichmentCOL1A12.31
62Epidermolysis bullosa, junctional 3b, severeEnrichmentLAMC22.31
63Epidermolysis bullosa, junctional 3a, intermediateEnrichmentLAMC22.31
64Polymicrogyria with or without vascular-type ehlers-danlos syndromeEnrichmentCOL3A12.31
65Nephrotic syndrome, type 5, with or without ocular abnormalitiesEnrichmentLAMB22.31
66Aortic dissectionEnrichmentCOL3A12.31
67Stickler syndrome, type iiEnrichmentCOL1A12.31
68Intermittent hydrarthrosisEnrichmentTNFRSF1A2.31
69Dentinogenesis imperfectaEnrichmentCOL1A22.31
70Familial thoracic aortic aneurysm and aortic dissectionEnrichmentCOL1A1, COL3A12.29
71Tuberous sclerosis 1EnrichmentIFNG2.14
72Severe combined immunodeficiency, x-linkedEnrichmentIL2RG2.14
73Agammaglobulinemia 1, autosomal recessiveEnrichmentIGHM2.14
74Glomerulopathy with fibronectin deposits 2EnrichmentFN12.14
75Combined immunodeficiency, x-linkedEnrichmentIL2RG2.14
76Hepatitis c virusEnrichmentIFNG2.14
77Caffey diseaseEnrichmentCOL1A12.14
78Tuberous sclerosis 2EnrichmentIFNG2.14
79Agammaglobulinemia 1EnrichmentIGHM2.14
80PhenylketonuriaEnrichmentCOL1A12.01
81Idiopathic aplastic anemiaEnrichmentIFNG1.92
82Familial cerebral saccular aneurysmEnrichmentCOL3A11.92
83Epidermolysis bullosa, junctional 1a, intermediateEnrichmentLAMC21.84
84Epidermolysis bullosa, junctional 1b, severeEnrichmentLAMC21.84
85Junctional epidermolysis bullosa non-herlitz typeEnrichmentLAMC21.84
86KeratoconusEnrichmentCOL1A11.84
87Common variable immunodeficiencyEnrichmentCD40LG1.77
88Spastic paraplegia 4, autosomal dominantEnrichmentCOL3A11.71
89Charge syndromeEnrichmentTNFRSF1A1.66
90Junctional epidermolysis bullosaEnrichmentLAMC21.66
91Familial thoracic aortic aneurysm and dissectionEnrichmentCOL3A11.66
92Omenn syndromeEnrichmentIL2RG1.62
93Aplastic anemiaEnrichmentIFNG1.62
94Autosomal non-syndromic agammaglobulinemiaEnrichmentIGHM1.62
95IchthyosisEnrichmentIL2RB1.58
96Presynaptic congenital myasthenic syndromesEnrichmentLAMA51.58
97Aortic aneurysm, familial thoracic 1EnrichmentCOL3A11.47
98Kidney diseaseEnrichmentLAMB21.44
99Human immunodeficiency virus type 1EnrichmentIFNG1.37
100Behcet syndromeEnrichmentTNFRSF1A1.34
101Skin diseaseEnrichmentLAMC21.28
102Autoinflammatory diseaseEnrichmentTNFRSF1A1.25
103Genetic steroid-resistant nephrotic syndromeEnrichmentLAMA51.10
104HypertelorismEnrichmentCOL1A10.92
105Primary ovarian insufficiencyEnrichmentTHBS10.87
106Breast cancerEnrichmentIL20.78

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