Cell interactions of the pancreatic cancer microenvironment

No Pathway Network information available for Cell interactions of the pancreatic cancer microenvironment

Pathways in the Cell interactions of the pancreatic cancer microenvironment SuperPath

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

Disorders associated with Cell interactions of the pancreatic cancer microenvironment SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Human immunodeficiency virus type 1EnrichmentCCL2, CCL5, CCR2, CCR5, CXCL129.64
2Vogt-koyanagi-harada diseaseEnrichmentFAS, HLA-DRB14.91
3Autoimmune lymphoproliferative syndromeEnrichmentFAS, FASLG4.61
4Precursor t-cell acute lymphoblastic leukemiaEnrichmentTRA, TRB2.99
5Lung cancerEnrichmentFAS, FASLG2.71
6Surfactant metabolism dysfunction, pulmonary, 4EnrichmentCSF2RA2.69
7Celiac disease 3EnrichmentCTLA42.69
8Polycystic lung diseaseEnrichmentCCR22.69
9Cardiomyopathy, dilated, 1hhEnrichmentBAG32.69
10Whim syndrome 1EnrichmentCXCR42.69
11Type 1 diabetes mellitus 12EnrichmentCTLA42.69
12Pulmonary alveolar proteinosis, acquiredEnrichmentHLA-DRB12.69
13Microvascular complications of diabetes 1EnrichmentVEGFA2.69
14Myopathy, myofibrillar, 6EnrichmentBAG32.69
15Graham little-piccardi-lassueur syndromeEnrichmentHLA-DRA2.69
16Type 1 diabetes mellitus 22EnrichmentCCR52.69
17Brain abnormalities, neurodegeneration, and dysosteosclerosisEnrichmentCSF1R2.69
18Tufted angioma of skinEnrichmentKDR2.69
19Csf1r-related disorderEnrichmentCSF1R2.69
20Charcot-marie-tooth disease, axonal, type 2jjEnrichmentBAG32.69
21Neuronopathy, distal hereditary motor, autosomal dominant 15EnrichmentBAG32.69
22Early-onset calcifying leukoencephalopathy-skeletal dysplasiaEnrichmentCSF1R2.69
23Systemic lupus erythematosusEnrichmentCTLA4, HLA-DRB12.54
24Hashimoto thyroiditisEnrichmentCTLA42.38
25Camurati-engelmann disease 1EnrichmentTGFB12.38
26West nile virusEnrichmentCCR52.38
27Sarcoidosis 1EnrichmentHLA-DRB12.38
28Angioma, tuftedEnrichmentKDR2.38
29Inflammatory bowel disease, immunodeficiency, and encephalopathyEnrichmentTGFB12.38
30Camurati-engelmann diseaseEnrichmentTGFB12.38
31Trypsinogen deficiencyEnrichmentTRB2.38
32Bullous pemphigoidEnrichmentHLA-DRB12.38
33Pediatric multiple sclerosisEnrichmentHLA-DRB12.38
34Mycosis fungoidesEnrichmentCTLA42.21
35Immunodeficiency 98 with autoinflammation, x-linkedEnrichmentFASLG2.21
36Leukoencephalopathy, hereditary diffuse, with spheroids 1EnrichmentCSF1R2.21
37Hepatitis c virusEnrichmentCCR52.21
38Immune dysregulation with autoimmunity, immunodeficiency, and lymphoproliferationEnrichmentCTLA42.21
39Asparagine synthetase deficiencyEnrichmentCTLA42.21
40Immunodeficiency 7EnrichmentTRA2.21
41Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndromeEnrichmentCTLA42.21
42Adult-onset myasthenia gravisEnrichmentCTLA42.21
43Saczary syndromeEnrichmentCTLA42.21
44Temporal arteritisEnrichmentHLA-DRB12.08
45Immunodeficiency, common variable, 1EnrichmentCTLA42.08
46Systemic-onset juvenile idiopathic arthritisEnrichmentHLA-DRB12.08
47Vitamin d-dependent rickets, type 2aEnrichmentTRB1.99
48Narcolepsy 2EnrichmentHLA-DRB11.99
49Follicular lymphomaEnrichmentHLA-DRB11.99
50Diffuse cutaneous systemic sclerosisEnrichmentHLA-DRB11.99
51Hereditary pulmonary alveolar proteinosisEnrichmentCSF2RA1.99
52Hemangioma, capillary infantileEnrichmentKDR1.91
53Inflammatory bowel disease 25, autosomal recessiveEnrichmentTGFB11.91
54Granulomatosis with polyangiitisEnrichmentCTLA41.91
55Limited sclerodermaEnrichmentHLA-DRB11.91
56Il10-related early-onset inflammatory bowel diseaseEnrichmentTGFB11.91
57Narcolepsy 1EnrichmentHLA-DRB11.79
58MyocarditisEnrichmentBAG31.79
59Frontotemporal dementia 1EnrichmentCSF1R1.65
60Alzheimer's diseaseEnrichmentCSF1R1.58
61Multiple sclerosisEnrichmentHLA-DRB11.54
62Hereditary chronic pancreatitisEnrichmentTRB1.54
63Alzheimer disease, familial, 1EnrichmentCSF1R1.46
64Pancreatitis, hereditaryEnrichmentTRB1.46
65Behcet syndromeEnrichmentFAS1.41
66Cardiomyopathy, dilated, 1aEnrichmentBAG31.37
67Tetralogy of fallotEnrichmentKDR1.28
68Cystic fibrosisEnrichmentTGFB11.19
69Peripheral nervous system diseaseEnrichmentBAG31.19
70NeuropathyEnrichmentBAG31.19
71Familial isolated dilated cardiomyopathyEnrichmentBAG30.98
72Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentCSF1R0.95
73Primary ovarian insufficiencyEnrichmentKDR0.94
74Dilated cardiomyopathyEnrichmentBAG30.82

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