Cancer immunotherapy by PD-1 blockade

No Pathway Network information available for Cancer immunotherapy by PD-1 blockade

Pathways in the Cancer immunotherapy by PD-1 blockade SuperPath

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

Disorders associated with Cancer immunotherapy by PD-1 blockade SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Severe combined immunodeficiencyEnrichmentCD3D, CD3E, CD3G, LCK, ZAP708.69
2T-b+ severe combined immunodeficiency due to cd3delta/cd3epsilon/cd3zetaEnrichmentCD3D, CD3E5.08
3Precursor t-cell acute lymphoblastic leukemiaEnrichmentTRA, TRB3.17
4MetachondromatosisEnrichmentPTPN112.77
5Leopard syndrome 1EnrichmentPTPN112.77
6Immunodeficiency 116EnrichmentCD8A2.77
7Immunodeficiency 69EnrichmentIFNG2.77
8Immunodeficiency 48EnrichmentZAP702.77
9Autoimmune disease, multisystem, infantile-onset, 4EnrichmentPDCD12.77
10T-cell large granular lymphocyte leukemiaEnrichmentSTAT32.77
11Immunodeficiency 18EnrichmentCD3E2.77
12Systemic lupus erythematosus 2EnrichmentPDCD12.77
13Autoimmune disease, multisystem, infantile-onset, 2EnrichmentZAP702.77
14Immunodeficiency 22EnrichmentLCK2.77
15Autoimmune disease, multisystem, infantile-onset, 1EnrichmentSTAT32.77
16Immunodeficiency 19, severe combinedEnrichmentCD3D2.77
17Autoimmune disease, multisystem, infantile-onset, 5EnrichmentCD2742.77
18Stat3-related early-onset multisystem autoimmune diseaseEnrichmentSTAT32.77
19Immunodeficiency 19EnrichmentCD3D2.77
20Chronic lymphoproliferative disorder of natural killer cellsEnrichmentSTAT32.77
21Inflammatory bowel disease-recurrent sinopulmonary infections syndromeEnrichmentNFAT52.77
22Zap70-related severe combined immunodeficiencyEnrichmentZAP702.77
23Malignant astrocytomaEnrichmentPTPN112.77
24Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.47
25Werner syndromeEnrichmentPTPN112.47
26Trypsinogen deficiencyEnrichmentTRB2.47
27Immunodeficiency 17EnrichmentCD3G2.47
28Joint contractures, osteochondromas, and b-cell lymphomaEnrichmentNFATC22.47
29Common variable immunodeficiency 12EnrichmentNFKB12.47
30Hyper-ige syndrome 1, autosomal dominant, with recurrent infectionsEnrichmentSTAT32.29
31Tuberous sclerosis 1EnrichmentIFNG2.29
32Hepatitis c virusEnrichmentIFNG2.29
33Tuberous sclerosis 2EnrichmentIFNG2.29
34Breast implant-associated anaplastic large cell lymphomaEnrichmentSTAT32.29
35Hyper ige syndromeEnrichmentSTAT32.29
36Immunodeficiency 7EnrichmentTRA2.29
37Tricuspid valve insufficiencyEnrichmentPTPN112.29
38Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentPTPN112.17
39Noonan syndrome with multiple lentiginesEnrichmentPTPN112.17
40Vitamin d-dependent rickets, type 2aEnrichmentTRB2.07
41LymphomaEnrichmentPTPN112.07
42Idiopathic aplastic anemiaEnrichmentIFNG2.07
43Patent ductus arteriosusEnrichmentPTPN111.99
44Noonan syndrome 3EnrichmentPTPN111.93
45Common variable immunodeficiencyEnrichmentNFKB11.93
46Permanent neonatal diabetes mellitusEnrichmentSTAT31.87
47Ciliary dyskinesia, primary, 3EnrichmentNFKB11.77
48Aplastic anemiaEnrichmentIFNG1.77
49Pectus excavatumEnrichmentPTPN111.73
50Combined immunodeficiencyEnrichmentZAP701.73
51Combined t cell and b cell immunodeficiencyEnrichmentZAP701.73
52Specific learning disabilityEnrichmentPTPN111.73
53Combined t and b cell immunodeficiencyEnrichmentZAP701.73
54EpicanthusEnrichmentPTPN111.70
55Juvenile myelomonocytic leukemiaEnrichmentPTPN111.70
56Congenital long qt syndromeEnrichmentPTPN111.70
57Acute promyelocytic leukemiaEnrichmentSTAT31.66
58Hereditary chronic pancreatitisEnrichmentTRB1.63
59Noonan syndrome and noonan-related syndromeEnrichmentPTPN111.60
60Pancreatitis, hereditaryEnrichmentTRB1.55
61Human immunodeficiency virus type 1EnrichmentIFNG1.52
62Patent foramen ovaleEnrichmentPTPN111.52
63Diffuse large b-cell lymphomaEnrichmentSTAT31.50
64Cardiomyopathy, dilated, 1aEnrichmentNFATC21.46
65Noonan syndrome 1EnrichmentPTPN111.42
66ScoliosisEnrichmentPTPN111.40
67Hydrops fetalis, nonimmuneEnrichmentPTPN111.36
68RasopathyEnrichmentPTPN111.36
69StrabismusEnrichmentPTPN111.35
70Long qt syndrome 1EnrichmentPTPN111.30
71Non-immune hydrops fetalisEnrichmentPTPN111.29
72Systemic lupus erythematosusEnrichmentPDCD11.19
73Hypertrophic cardiomyopathyEnrichmentPTPN111.15
74ThrombocytopeniaEnrichmentPTPN111.11
75Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentPTPN111.04
76Breast cancerEnrichmentJUN0.92
77Autism spectrum disorderEnrichmentPTPN110.77
78MicrocephalyEnrichmentPTPN110.72
79Inherited cancer-predisposing syndromeEnrichmentPTPN110.70

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