IL1 and megakaryocytes in obesity

No Pathway Network information available for IL1 and megakaryocytes in obesity

Pathways in the IL1 and megakaryocytes in obesity SuperPath

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

Disorders associated with IL1 and megakaryocytes in obesity SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Human immunodeficiency virus type 1EnrichmentCCL2, IFNG3.35
2MacrodactylyEnrichmentPIK3CA2.75
3Leprosy 3EnrichmentTLR22.75
4Cinca syndromeEnrichmentNLRP32.75
5Immunodeficiency 68EnrichmentMYD882.75
6Keratoendotheliitis fugax hereditariaEnrichmentNLRP32.75
7Macroglobulinemia, waldenstrom 1EnrichmentMYD882.75
8Megalencephaly, autosomal dominantEnrichmentPIK3CA2.75
9Prothrombin deficiency, congenitalEnrichmentF22.75
10Familial cold autoinflammatory syndrome 1EnrichmentNLRP32.75
11Cowden syndrome 5EnrichmentPIK3CA2.75
12Leprosy 5EnrichmentTLR12.75
13Muckle-wells syndromeEnrichmentNLRP32.75
14Cerebral cavernous malformations 4EnrichmentPIK3CA2.75
15Immunodeficiency 69EnrichmentIFNG2.75
16Deafness, autosomal dominant 34, with or without inflammationEnrichmentNLRP32.75
17Chronic recurrent multifocal osteomyelitis 3EnrichmentIL1R12.75
18Hemifacial myohyperplasiaEnrichmentPIK3CA2.75
19Capillary malformation of the lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs, and partial/generalized overgrowthEnrichmentPIK3CA2.75
20Pregnancy loss, recurrent 2EnrichmentF22.75
21Platelet-activating factor acetylhydrolase deficiencyEnrichmentPLA2G72.75
22Extraoral halitosis due to methanethiol oxidase deficiencyEnrichmentSELENBP12.75
23Segmental progressive overgrowth syndrome with fibroadipose hyperplasiaEnrichmentPIK3CA2.75
24HypospadiasEnrichmentPIK3CA2.75
25Prothrombin deficiencyEnrichmentF22.75
26Rare venous malformationEnrichmentPIK3CA2.75
27Diaphragmatic eventrationEnrichmentPIK3CA2.75
28Waldenstram macroglobulinemiaEnrichmentMYD882.75
29Pik3ca-related overgrowth spectrumEnrichmentPIK3CA2.75
30Cryopyrin associated periodic syndromeEnrichmentNLRP32.75
31Rare combined vascular malformationEnrichmentPIK3CA2.75
32Cavernous lymphangiomaEnrichmentPIK3CA2.75
33Pik3ca-related overgrowth syndromeEnrichmentPIK3CA2.75
34Familial amyloid nephropathy with urticaria and deafnessEnrichmentNLRP32.75
35Hemihyperplasia-multiple lipomatosis syndromeEnrichmentPIK3CA2.75
36Eccrine angiomatous hamartomaEnrichmentPIK3CA2.75
37Macrodactyly of toeEnrichmentPIK3CA2.75
38Gastric cancerEnrichmentIL1B, PIK3CA2.59
39Keratosis, seborrheicEnrichmentPIK3CA2.45
40Noonan syndrome 8EnrichmentPIK3CA2.45
41Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.45
42Rosette-forming glioneuronal tumorEnrichmentPIK3CA2.45
43Metaphyseal anadysplasia 2EnrichmentMMP92.45
44Pericardial effusionEnrichmentNLRP32.45
45Metaphyseal anadysplasiaEnrichmentMMP92.45
46Transient predisposition to invasive pyogenic bacterial infectionEnrichmentMYD882.45
47Common variable immunodeficiency 12EnrichmentNFKB12.45
48Pompe disease, infantile-onsetEnrichmentPIK3CA2.28
49Tuberous sclerosis 1EnrichmentIFNG2.28
50Hepatitis c virusEnrichmentIFNG2.28
51Congenital lipomatous overgrowth, vascular malformations, and epidermal neviEnrichmentPIK3CA2.28
52Tuberous sclerosis 2EnrichmentIFNG2.28
53KeratoacanthomaEnrichmentPIK3CA2.28
54Cerebral sinovenous thrombosisEnrichmentF22.28
55Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentPIK3CA2.15
56Cerebrovascular diseaseEnrichmentPIK3CA2.15
57Familial cerebral cavernous malformationsEnrichmentPIK3CA2.15
58Cerebral malariaEnrichmentICAM12.15
59Pediatric systemic lupus erythematosusEnrichmentIRAK12.15
60Capillary malformations, congenitalEnrichmentPIK3CA2.05
61HemimegalencephalyEnrichmentPIK3CA2.05
62Idiopathic aplastic anemiaEnrichmentIFNG2.05
63Colorectal cancerEnrichmentPIK3CA, TLR21.99
64Klippel-trenaunay-weber syndromeEnrichmentPIK3CA1.98
65Cowden syndrome 1EnrichmentPIK3CA1.98
66Hemihyperplasia, isolatedEnrichmentPIK3CA1.98
67Breast adenocarcinomaEnrichmentPIK3CA1.98
68Lung squamous cell carcinomaEnrichmentPIK3CA1.98
69Nevus, epidermalEnrichmentPIK3CA1.91
70Thrombophilia due to thrombin defectEnrichmentF21.91
71Capillary malformation-arteriovenous malformation 1EnrichmentPIK3CA1.91
72Gallbladder cancerEnrichmentPIK3CA1.91
73Common variable immunodeficiencyEnrichmentNFKB11.91
74Rheumatoid arthritisEnrichmentTLR11.80
75Arteriovenous malformationEnrichmentPIK3CA1.80
76Adult hepatocellular carcinomaEnrichmentPIK3CA1.80
77Cowden syndromeEnrichmentPIK3CA1.80
78Stroke, ischemicEnrichmentF21.76
79Myopathy, x-linked, with excessive autophagyEnrichmentPIK3CA1.76
80Ciliary dyskinesia, primary, 3EnrichmentNFKB11.76
81Aplastic anemiaEnrichmentIFNG1.76
82Lung non-small cell carcinomaEnrichmentPIK3CA1.71
83MeningiomaEnrichmentPIK3CA1.68
84Lip and oral cavity carcinomaEnrichmentPIK3CA1.68
85Lynch syndromeEnrichmentPIK3CA1.58
86Arteriovenous malformations of the brainEnrichmentNLRP31.48
87Diffuse large b-cell lymphomaEnrichmentMYD881.48
88Endometrial cancerEnrichmentPIK3CA1.44
89Hepatocellular carcinomaEnrichmentPIK3CA1.42
90MalariaEnrichmentICAM11.40
91Autoinflammatory diseaseEnrichmentNLRP31.38
92Bladder cancerEnrichmentPIK3CA1.30
93Prostate cancerEnrichmentPIK3CA1.30
94Lung cancerEnrichmentPIK3CA1.26
95Systemic lupus erythematosusEnrichmentIRAK11.18
96Cerebral palsyEnrichmentF21.18
97Hereditary breast carcinomaEnrichmentPIK3CA1.12
98HypertelorismEnrichmentPIK3CA1.05
99Breast cancerEnrichmentPIK3CA0.90
100Ovarian cancerEnrichmentPIK3CA0.78

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