Extracellular vesicles in the crosstalk of cardiac cells

No Pathway Network information available for Extracellular vesicles in the crosstalk of cardiac cells

Pathways in the Extracellular vesicles in the crosstalk of cardiac cells SuperPath

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

Disorders associated with Extracellular vesicles in the crosstalk of cardiac cells SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Cowden syndrome 1EnrichmentEGFR, PTEN4.43
2Squamous cell carcinoma, head and neckEnrichmentEGFR, PTEN4.28
3Arteriovenous malformations of the brainEnrichmentEGFR, IL63.37
4Diffuse large b-cell lymphomaEnrichmentPTEN, STAT33.37
5Tetralogy of fallotEnrichmentGATA4, KDR3.10
6Bladder cancerEnrichmentEGFR, PTEN3.00
7Vacterl association with hydrocephalusEnrichmentPTEN2.79
8Hypomagnesemia 4, renalEnrichmentEGF2.79
9Immunodeficiency, common variable, 6EnrichmentCD812.79
10Atrioventricular septal defect 4EnrichmentGATA42.79
11T-cell large granular lymphocyte leukemiaEnrichmentSTAT32.79
12Papillary tumor of the pineal regionEnrichmentPTEN2.79
13Charcot-marie-tooth disease, axonal, type 2fEnrichmentHSPB12.79
14Atrial septal defect 2EnrichmentGATA42.79
15Testicular anomalies with or without congenital heart diseaseEnrichmentGATA42.79
16Macular degeneration, age-related, 10EnrichmentTLR42.79
17Glioma susceptibility 2EnrichmentPTEN2.79
18Autoimmune disease, multisystem, infantile-onset, 1EnrichmentSTAT32.79
198p23.1 microdeletion syndromeEnrichmentGATA42.79
20Tufted angioma of skinEnrichmentKDR2.79
21Stat3-related early-onset multisystem autoimmune diseaseEnrichmentSTAT32.79
22Partial atrioventricular septal defect with ventricular hypoplasiaEnrichmentGATA42.79
23Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndromeEnrichmentPTEN2.79
24Chronic lymphoproliferative disorder of natural killer cellsEnrichmentSTAT32.79
25Egf-related primary hypomagnesemia with intellectual disabilityEnrichmentEGF2.79
26Neuronopathy, distal hereditary motor, autosomal dominant 3EnrichmentHSPB12.49
27Angioma, tuftedEnrichmentKDR2.49
2846,xy sex reversal 3EnrichmentGATA42.49
29Metaphyseal anadysplasia 2EnrichmentMMP92.49
30Spastic tetraplegia and axial hypotonia, progressiveEnrichmentSOD12.49
31Metaphyseal anadysplasiaEnrichmentMMP92.49
32Common variable immunodeficiency phenotype due to cd19/cd81 deficiencyEnrichmentCD812.49
33Vacterl with hydrocephalusEnrichmentPTEN2.49
34Growth delay due to insulin-like growth factor type 1 deficiencyEnrichmentIGF12.49
35Juvenile polyposis of infancyEnrichmentPTEN2.49
36Hyper-ige syndrome 1, autosomal dominant, with recurrent infectionsEnrichmentSTAT32.31
37Neonatal nephrocutaneous inflammatory syndromeEnrichmentEGFR2.31
38Breast implant-associated anaplastic large cell lymphomaEnrichmentSTAT32.31
39Hyper ige syndromeEnrichmentSTAT32.31
40Laryngeal squamous cell carcinomaEnrichmentPTEN2.31
41Neonatal inflammatory skin and bowel diseaseEnrichmentEGFR2.31
42Kaposi sarcomaEnrichmentIL62.19
43Pediatric systemic lupus erythematosusEnrichmentSPP12.19
44Transposition of the great arteriesEnrichmentGATA42.19
45Systemic-onset juvenile idiopathic arthritisEnrichmentIL62.19
46GliomaEnrichmentPTEN2.19
47Neuronopathy, distal hereditary motor, autosomal dominant 2EnrichmentHSPB12.09
48Macrocephaly/autism syndromeEnrichmentPTEN2.09
49Rheumatoid arthritis, systemic juvenileEnrichmentIL62.09
50Insulin-like growth factor iEnrichmentIGF12.09
51Amyotrophic lateral sclerosis 10 with or without frontotemporal dementiaEnrichmentSOD12.09
52Ventricular septal defect 1EnrichmentGATA42.09
53Congenital heart defects, multiple types, 4EnrichmentGATA42.09
54HemangiomaEnrichmentPTEN2.09
55Acute megakaryocytic leukemiaEnrichmentPTEN2.09
56HemimegalencephalyEnrichmentPTEN2.09
57Type 1 diabetes mellitusEnrichmentIL62.01
58Hemangioma, capillary infantileEnrichmentKDR2.01
59Lung squamous cell carcinomaEnrichmentEGFR2.01
60Thyroid cancer, nonmedullary, 2EnrichmentPTEN1.95
61Fundus albipunctatusEnrichmentCD631.95
62Motor neuron diseaseEnrichmentSOD11.95
63Follicular thyroid carcinomaEnrichmentPTEN1.95
64Ovarian cancerEnrichmentEGFR, PTEN1.94
65Permanent neonatal diabetes mellitusEnrichmentSTAT31.89
66Inflammatory bowel disease 1EnrichmentIL61.84
67Adult hepatocellular carcinomaEnrichmentEGF1.84
68Cowden syndromeEnrichmentPTEN1.84
69Amyotrophic lateral sclerosis 1EnrichmentSOD11.79
70MelanomaEnrichmentPTEN1.79
71Meningioma, familialEnrichmentPTEN1.75
72Lung non-small cell carcinomaEnrichmentEGFR1.75
73Uterine corpus cancerEnrichmentPTEN1.75
74Inherited cancer-predisposing syndromeEnrichmentEGFR, PTEN1.72
75MeningiomaEnrichmentPTEN1.71
76Lip and oral cavity carcinomaEnrichmentEGFR1.71
77Acute promyelocytic leukemiaEnrichmentSTAT31.68
78Aortic aneurysm, familial thoracic 1EnrichmentGATA41.65
79Lung cancer susceptibility 3EnrichmentEGFR1.65
80Heart diseaseEnrichmentGATA41.65
8146,xy partial gonadal dysgenesisEnrichmentGATA41.65
82RhabdomyosarcomaEnrichmentPTEN1.59
83GliosarcomaEnrichmentEGFR1.59
84Giant cell glioblastomaEnrichmentEGFR1.56
85Heart, malformation ofEnrichmentGATA41.54
86Patent foramen ovaleEnrichmentGATA41.54
87Behcet syndromeEnrichmentTLR41.52
88Endometrial cancerEnrichmentPTEN1.47
89Congenital stationary night blindnessEnrichmentCD631.44
90Familial atrial fibrillationEnrichmentGATA41.42
91Prostate cancerEnrichmentPTEN1.34
92Lung cancerEnrichmentEGFR1.30
93Systemic lupus erythematosusEnrichmentSPP11.21
94Charcot-marie-tooth diseaseEnrichmentHSPB11.19
95Type 2 diabetes mellitusEnrichmentIL61.18
96Gastric cancerEnrichmentPTEN1.17
97Hereditary breast carcinomaEnrichmentPTEN1.16
98Hereditary breast ovarian cancer syndromeEnrichmentPTEN1.07
99Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentGATA41.06
100Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentSOD11.05
101Primary ovarian insufficiencyEnrichmentKDR1.04
102Breast cancerEnrichmentPTEN0.94
103Congenital nervous system abnormalityEnrichmentPTEN0.80
104Nervous system diseaseEnrichmentPTEN0.80
105Autism spectrum disorderEnrichmentPTEN0.79
106Hereditary retinal dystrophyEnrichmentCD630.42
107Fundus dystrophyEnrichmentCD630.42

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