Cancer immunotherapy by CTLA4 blockade

No Pathway Network information available for Cancer immunotherapy by CTLA4 blockade

Pathways in the Cancer immunotherapy by CTLA4 blockade SuperPath

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

Disorders associated with Cancer immunotherapy by CTLA4 blockade SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Mycosis fungoidesEnrichmentCD28, CTLA45.47
2Congenital lipomatous overgrowth, vascular malformations, and epidermal neviEnrichmentPIK3CA, PIK3R15.47
3Immunodeficiency 14a with lymphoproliferation, autosomal dominantEnrichmentPIK3CD, PIK3R15.47
4Immunodeficiency 14EnrichmentPIK3CD, PIK3R15.47
5Saczary syndromeEnrichmentCD28, CTLA45.47
6Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentPIK3CA, PIK3R25.16
7Autosomal non-syndromic agammaglobulinemiaEnrichmentPIK3CD, PIK3R14.29
8Precursor t-cell acute lymphoblastic leukemiaEnrichmentTRA, TRB3.55
9MacrodactylyEnrichmentPIK3CA2.96
10MetachondromatosisEnrichmentPTPN112.96
11Celiac disease 3EnrichmentCTLA42.96
12Megalencephaly, autosomal dominantEnrichmentPIK3CA2.96
13Leopard syndrome 1EnrichmentPTPN112.96
14Cowden syndrome 5EnrichmentPIK3CA2.96
15Cerebral cavernous malformations 4EnrichmentPIK3CA2.96
16Short syndromeEnrichmentPIK3R12.96
17Type 1 diabetes mellitus 12EnrichmentCTLA42.96
18Hemifacial myohyperplasiaEnrichmentPIK3CA2.96
19Capillary malformation of the lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs, and partial/generalized overgrowthEnrichmentPIK3CA2.96
20Immunodeficiency 36 with lymphoproliferationEnrichmentPIK3R12.96
21Immunodeficiency 14b, autosomal recessiveEnrichmentPIK3CD2.96
22Agammaglobulinemia 7, autosomal recessiveEnrichmentPIK3R12.96
23Immunodeficiency 123 with hpv-related verrucosisEnrichmentCD282.96
24Segmental progressive overgrowth syndrome with fibroadipose hyperplasiaEnrichmentPIK3CA2.96
25HypospadiasEnrichmentPIK3CA2.96
26Rare venous malformationEnrichmentPIK3CA2.96
27Vegetative pyoderma gangrenosumEnrichmentPTPN62.96
28Bullous pyoderma gangrenosumEnrichmentPTPN62.96
29Diaphragmatic eventrationEnrichmentPIK3CA2.96
30Pustular pyoderma gangrenosumEnrichmentPTPN62.96
31Pik3ca-related overgrowth spectrumEnrichmentPIK3CA2.96
32Rare combined vascular malformationEnrichmentPIK3CA2.96
33Cavernous lymphangiomaEnrichmentPIK3CA2.96
34Pik3ca-related overgrowth syndromeEnrichmentPIK3CA2.96
35Classic pyoderma gangrenosumEnrichmentPTPN62.96
36Hemihyperplasia-multiple lipomatosis syndromeEnrichmentPIK3CA2.96
37Eccrine angiomatous hamartomaEnrichmentPIK3CA2.96
38Macrodactyly of toeEnrichmentPIK3CA2.96
39Malignant astrocytomaEnrichmentPTPN112.96
40Hashimoto thyroiditisEnrichmentCTLA42.66
41Keratosis, seborrheicEnrichmentPIK3CA2.66
42Roifman-chitayat syndromeEnrichmentPIK3CD2.66
43Noonan syndrome 8EnrichmentPIK3CA2.66
44Werner syndromeEnrichmentPTPN112.66
45Rosette-forming glioneuronal tumorEnrichmentPIK3CA2.66
46Trypsinogen deficiencyEnrichmentTRB2.66
47Immune system diseaseEnrichmentPIK3CD2.66
48Houge-janssens syndrome 3EnrichmentPPP2CA2.66
49Pompe disease, infantile-onsetEnrichmentPIK3CA2.48
50Neutrophilic dermatosis, acute febrileEnrichmentPTPN62.48
51Immune dysregulation with autoimmunity, immunodeficiency, and lymphoproliferationEnrichmentCTLA42.48
52Asparagine synthetase deficiencyEnrichmentCTLA42.48
53Immunodeficiency 7EnrichmentTRA2.48
54Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndromeEnrichmentCTLA42.48
55Adult-onset myasthenia gravisEnrichmentCTLA42.48
56Tricuspid valve insufficiencyEnrichmentPTPN112.48
57KeratoacanthomaEnrichmentPIK3CA2.48
58Colorectal cancerEnrichmentPIK3CA, PIK3R12.39
59Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1EnrichmentPIK3R22.35
60Immunodeficiency, common variable, 1EnrichmentCTLA42.35
61Cerebrovascular diseaseEnrichmentPIK3CA2.35
62Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentPTPN112.35
63Noonan syndrome with multiple lentiginesEnrichmentPTPN112.35
64Familial cerebral cavernous malformationsEnrichmentPIK3CA2.35
65Capillary malformations, congenitalEnrichmentPIK3CA2.26
66Vitamin d-dependent rickets, type 2aEnrichmentTRB2.26
67LymphomaEnrichmentPTPN112.26
68HemimegalencephalyEnrichmentPIK3CA2.26
69Klippel-trenaunay-weber syndromeEnrichmentPIK3CA2.18
70Cowden syndrome 1EnrichmentPIK3CA2.18
71Hemihyperplasia, isolatedEnrichmentPIK3CA2.18
72Granulomatosis with polyangiitisEnrichmentCTLA42.18
73Patent ductus arteriosusEnrichmentPTPN112.18
74Breast adenocarcinomaEnrichmentPIK3CA2.18
75Lung squamous cell carcinomaEnrichmentPIK3CA2.18
76Nevus, epidermalEnrichmentPIK3CA2.11
77Capillary malformation-arteriovenous malformation 1EnrichmentPIK3CA2.11
78Noonan syndrome 3EnrichmentPTPN112.11
79Gallbladder cancerEnrichmentPIK3CA2.11
80Overgrowth syndromeEnrichmentPIK3R12.11
81Arteriovenous malformationEnrichmentPIK3CA2.00
82Adult hepatocellular carcinomaEnrichmentPIK3CA2.00
83Cowden syndromeEnrichmentPIK3CA2.00
84Myopathy, x-linked, with excessive autophagyEnrichmentPIK3CA1.96
85Pectus excavatumEnrichmentPTPN111.92
86Lung non-small cell carcinomaEnrichmentPIK3CA1.92
87Specific learning disabilityEnrichmentPTPN111.92
88EpicanthusEnrichmentPTPN111.88
89Juvenile myelomonocytic leukemiaEnrichmentPTPN111.88
90MeningiomaEnrichmentPIK3CA1.88
91Lip and oral cavity carcinomaEnrichmentPIK3CA1.88
92Congenital long qt syndromeEnrichmentPTPN111.88
93Nk-cell enteropathyEnrichmentPIK3CB1.85
94Hereditary chronic pancreatitisEnrichmentTRB1.81
95Lynch syndromeEnrichmentPIK3CA1.78
96Noonan syndrome and noonan-related syndromeEnrichmentPTPN111.78
97Pancreatitis, hereditaryEnrichmentTRB1.73
98Patent foramen ovaleEnrichmentPTPN111.70
99Endometrial cancerEnrichmentPIK3CA1.64
100Hepatocellular carcinomaEnrichmentPIK3CA1.62
101Noonan syndrome 1EnrichmentPTPN111.60
102ScoliosisEnrichmentPTPN111.58
103Hydrops fetalis, nonimmuneEnrichmentPTPN111.55
104RasopathyEnrichmentPTPN111.55
105StrabismusEnrichmentPTPN111.53
106Bladder cancerEnrichmentPIK3CA1.50
107Prostate cancerEnrichmentPIK3CA1.50
108Long qt syndrome 1EnrichmentPTPN111.49
109Non-immune hydrops fetalisEnrichmentPTPN111.47
110Lung cancerEnrichmentPIK3CA1.46
111Systemic lupus erythematosusEnrichmentCTLA41.37
112Gastric cancerEnrichmentPIK3CA1.33
113Hypertrophic cardiomyopathyEnrichmentPTPN111.33
114Hereditary breast carcinomaEnrichmentPIK3CA1.32
115ThrombocytopeniaEnrichmentPTPN111.29
116HypertelorismEnrichmentPIK3CA1.25
117Myeloma, multipleEnrichmentPIK3R21.22
118Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentPTPN111.22
119Breast cancerEnrichmentPIK3CA1.10
120Ovarian cancerEnrichmentPIK3CA0.97
121Autism spectrum disorderEnrichmentPTPN110.94
122MicrocephalyEnrichmentPTPN110.89
123Complex neurodevelopmental disorderEnrichmentPPP2CA0.89
124Inherited cancer-predisposing syndromeEnrichmentPTPN110.86

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