Inflammatory bowel disease signaling

No Pathway Network information available for Inflammatory bowel disease signaling

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

Disorders associated with Inflammatory bowel disease signaling SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Behcet syndromeEnrichmentIFNGR1, IL10, IL12A, IL23R, NOD2, STAT4, TLR410.48
2Immunodeficiency 31cEnrichmentIL21R, STAT15.03
3Il10-related early-onset inflammatory bowel diseaseEnrichmentIL10, TGFB14.66
4AsthmaEnrichmentIL13, TNF4.09
5Type 1 diabetes mellitusEnrichmentFOXP3, IL63.86
6Chronic mucocutaneous candidiasisEnrichmentIL17F, STAT13.86
7Human immunodeficiency virus type 1EnrichmentIFNG, IL103.65
8Systemic lupus erythematosusEnrichmentIL10, STAT4, TNF3.63
9Inflammatory bowel disease 1EnrichmentIL6, NOD23.48
10Primary biliary cholangitisEnrichmentIL12A, IL12RB13.48
11Leprosy 3EnrichmentTLR22.90
12Immunodysregulation, polyendocrinopathy, and enteropathy, x-linkedEnrichmentFOXP32.90
13Cataract 21, multiple typesEnrichmentMAF2.90
14Blau syndromeEnrichmentNOD22.90
15Immunodeficiency 69EnrichmentIFNG2.90
16Hyper-ige syndrome 6, autosomal dominant, with recurrent infectionsEnrichmentSTAT62.90
17Graft-versus-host diseaseEnrichmentIL102.90
18Ayme-gripp syndromeEnrichmentMAF2.90
19Allergic rhinitisEnrichmentIL132.90
20Hypoparathyroidism, sensorineural deafness, and renal dysplasia syndromeEnrichmentGATA32.60
21Camurati-engelmann disease 1EnrichmentTGFB12.60
22Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephalyEnrichmentFOXP32.60
23Hemangiopericytoma, malignantEnrichmentSTAT62.60
24Developmental and epileptic encephalopathy 28EnrichmentMAF2.60
25Yao syndromeEnrichmentNOD22.60
26Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.60
27Spinocerebellar ataxia, autosomal recessive 12EnrichmentMAF2.60
28Inflammatory bowel disease, immunodeficiency, and encephalopathyEnrichmentTGFB12.60
29Immunodeficiency 127EnrichmentTNF2.60
30Camurati-engelmann diseaseEnrichmentTGFB12.60
31B-lymphoblastic leukemia/lymphoma with hyperdiploidyEnrichmentGATA32.60
32Hypoparathyroidism-deafness-renal disease syndromeEnrichmentGATA32.60
33Crohn's diseaseEnrichmentNOD22.60
34Autosomal dominant nonsyndromic deafnessEnrichmentGATA32.60
35Common variable immunodeficiency 12EnrichmentNFKB12.60
36Helicobacter pylori infectionEnrichmentIFNGR12.51
37Legionnaire diseaseEnrichmentTLR52.51
38Immunodeficiency 30EnrichmentIL12RB12.51
39Candidiasis, familial, 6EnrichmentIL17F2.51
40Immunodeficiency 27aEnrichmentIFNGR12.51
41Disabling pansclerotic morphea of childhoodEnrichmentSTAT42.51
42Systemic lupus erythematosus 1EnrichmentTLR52.51
43T-cell large granular lymphocyte leukemiaEnrichmentSTAT32.51
44Systemic lupus erythematosus 11EnrichmentSTAT42.51
45Immunodeficiency 42EnrichmentRORC2.51
46Immunodeficiency 27bEnrichmentIFNGR12.51
47Psoriasis 7EnrichmentIL23R2.51
48Immunodeficiency 31aEnrichmentSTAT12.51
49MelioidosisEnrichmentTLR52.51
50Loeys-dietz syndrome 6EnrichmentSMAD22.51
51Inflammatory bowel disease 17EnrichmentIL23R2.51
52Macular degeneration, age-related, 10EnrichmentTLR42.51
53Immunodeficiency 31bEnrichmentSTAT12.51
54Autoimmune disease, multisystem, infantile-onset, 1EnrichmentSTAT32.51
55Immunodeficiency 88EnrichmentTBX212.51
56Congenital heart defects, multiple types, 8, with or without heterotaxyEnrichmentSMAD22.51
57Stat3-related early-onset multisystem autoimmune diseaseEnrichmentSTAT32.51
58Chronic lymphoproliferative disorder of natural killer cellsEnrichmentSTAT32.51
59Tuberous sclerosis 1EnrichmentIFNG2.43
60Severe combined immunodeficiency, x-linkedEnrichmentIL2RG2.43
61Combined immunodeficiency, x-linkedEnrichmentIL2RG2.43
62Psoriatic arthritisEnrichmentTNF2.43
63Hepatitis c virusEnrichmentIFNG2.43
64Tuberous sclerosis 2EnrichmentIFNG2.43
65Migraine without auraEnrichmentTNF2.43
66End stage renal diseaseEnrichmentGATA32.43
67Congenital blue dot cataractEnrichmentMAF2.30
68Cerebral malariaEnrichmentTNF2.30
69Immunodeficiency 56EnrichmentIL21R2.21
70Intellectual developmental disorder with or without epilepsy or cerebellar ataxiaEnrichmentRORA2.21
71Vascular dementiaEnrichmentTNF2.20
72Idiopathic aplastic anemiaEnrichmentIFNG2.20
73Inflammatory bowel disease 25, autosomal recessiveEnrichmentTGFB12.13
74Common variable immunodeficiencyEnrichmentNFKB12.06
75Hyper-ige syndrome 1, autosomal dominant, with recurrent infectionsEnrichmentSTAT32.03
76Asthma, nasal polyps, and aspirin intoleranceEnrichmentTBX212.03
77Breast implant-associated anaplastic large cell lymphomaEnrichmentSTAT32.03
78Hyper ige syndromeEnrichmentSTAT32.03
79Loeys-dietz syndrome 1EnrichmentSMAD22.03
80Immunodeficiency, common variable, 11EnrichmentIL212.03
81Cataract - microcornea syndromeEnrichmentMAF2.00
82Rheumatoid arthritisEnrichmentIL101.95
83Hydrops fetalisEnrichmentFOXP31.95
84Kaposi sarcomaEnrichmentIL61.91
85Hepatitis bEnrichmentIFNGR11.91
86Pediatric systemic lupus erythematosusEnrichmentSTAT41.91
87Systemic-onset juvenile idiopathic arthritisEnrichmentIL61.91
88Cataract 30, multiple typesEnrichmentMAF1.90
89Omenn syndromeEnrichmentIL2RG1.90
90Ciliary dyskinesia, primary, 3EnrichmentNFKB11.90
91Aplastic anemiaEnrichmentIFNG1.90
92Combined immunodeficiencyEnrichmentIL2RG1.86
93Combined t cell and b cell immunodeficiencyEnrichmentIL2RG1.86
94Combined t and b cell immunodeficiencyEnrichmentIL2RG1.86
95Rheumatoid arthritis, systemic juvenileEnrichmentIL61.81
96Alzheimer's diseaseEnrichmentTNF1.79
97Oligoarticular juvenile idiopathic arthritisEnrichmentSTAT41.67
98Rheumatoid factor-negative juvenile idiopathic arthritisEnrichmentSTAT41.67
99Breast cancerEnrichmentIL2, JUN1.65
100Permanent neonatal diabetes mellitusEnrichmentSTAT31.61
101Centronuclear myopathyEnrichmentFOXP31.58
102Loeys-dietz syndromeEnrichmentSMAD21.56
103MalariaEnrichmentTNF1.55
104Autoinflammatory diseaseEnrichmentNOD21.53
105Developmental and epileptic encephalopathy 1EnrichmentMAF1.51
106Cystic fibrosisEnrichmentTGFB11.40
107Acute promyelocytic leukemiaEnrichmentSTAT31.40
108CakutEnrichmentGATA31.38
109Benign epilepsy with centrotemporal spikesEnrichmentMAF1.30
110Centralopathic epilepsyEnrichmentMAF1.28
111West syndromeEnrichmentMAF1.27
112Arteriovenous malformations of the brainEnrichmentIL61.24
113Diffuse large b-cell lymphomaEnrichmentSTAT31.24
114Colorectal cancerEnrichmentTLR20.98
115Type 2 diabetes mellitusEnrichmentIL60.91
116Familial thoracic aortic aneurysm and aortic dissectionEnrichmentSMAD20.89
117Complex neurodevelopmental disorderEnrichmentRORA0.49

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