Prostaglandin and leukotriene metabolism in senescence

No Pathway Network information available for Prostaglandin and leukotriene metabolism in senescence

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

Disorders associated with Prostaglandin and leukotriene metabolism in senescence SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Lip and oral cavity carcinomaEnrichmentHRAS, RB13.60
2Bladder cancerEnrichmentHRAS, RB12.82
3Pseudohypoparathyroidism, type icEnrichmentGNAS2.70
4Osseous heteroplasia, progressiveEnrichmentGNAS2.70
5Ghosal hematodiaphyseal dysplasiaEnrichmentTBXAS12.70
6Sturge-weber syndromeEnrichmentGNAQ2.70
7Leukotriene c4 synthase deficiencyEnrichmentLTC4S2.70
8Acth-independent macronodular adrenal hyperplasia 1EnrichmentGNAS2.70
9Pituitary adenoma 3, multiple typesEnrichmentGNAS2.70
10Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalitiesEnrichmentGNAI12.70
11Cytosolic phospholipase-a2 alpha deficiency associated bleeding disorderEnrichmentPLA2G4A2.70
12Disorders of gnas inactivationEnrichmentGNAS2.70
13Gastrointestinal ulceration, recurrent, with dysfunctional plateletsEnrichmentPLA2G4A2.70
14Trilateral retinoblastomaEnrichmentRB12.70
15AtherosclerosisEnrichmentALOX52.70
16Cryptogenic multifocal ulcerous stenosing enteritisEnrichmentPLA2G4A2.70
17Monostotic fibrous dysplasiaEnrichmentGNAS2.70
18Phakomatosis pigmentokeratoticaEnrichmentHRAS2.70
19Mazabraud syndromeEnrichmentGNAS2.70
20Lung oat cell carcinomaEnrichmentRB12.70
21Pseudohypoparathyroidism, type iaEnrichmentGNAS2.40
22Costello syndromeEnrichmentHRAS2.40
23Pigmented nodular adrenocortical disease, primary, 1EnrichmentGNAS2.40
24PseudopseudohypoparathyroidismEnrichmentGNAS2.40
25Chromosome 13q14 deletion syndromeEnrichmentRB12.40
26Bleeding disorder, platelet-type, 14EnrichmentTBXAS12.40
27PseudohypoparathyroidismEnrichmentGNAS2.40
28Acth-independent macronodular adrenal hyperplasiaEnrichmentGNAS2.40
29Familial retinoblastomaEnrichmentRB12.40
30Phakomatosis cesioflammeaEnrichmentGNAQ2.40
31Wooly hair nevusEnrichmentHRAS2.40
32Mccune-albright syndromeEnrichmentGNAS2.22
33RetinoblastomaEnrichmentRB12.22
34Asthma, nasal polyps, and aspirin intoleranceEnrichmentPTGER22.22
35Osteogenic sarcomaEnrichmentRB12.22
36Woolly hair, autosomal recessive 3EnrichmentRB12.22
37Hypotrichosis 8EnrichmentRB12.22
38Large congenital melanocytic nevusEnrichmentHRAS2.22
39Squamous cell carcinomaEnrichmentRB12.22
40Bone osteosarcomaEnrichmentRB12.22
41SpermatocytomaEnrichmentHRAS2.22
42Cushing syndrome due to bilateral macronodular adrenocortical diseaseEnrichmentGNAS2.22
43Anastomosing haemangiomaEnrichmentGNAQ2.22
44Schimmelpenning-feuerstein-mims syndromeEnrichmentHRAS2.10
45Small cell cancer of the lungEnrichmentRB12.10
46Pseudohypoparathyroidism, type ibEnrichmentGNAS2.10
47Lynch syndrome 4EnrichmentRB12.10
48Epidermolytic nevusEnrichmentHRAS2.10
49Capillary malformations, congenitalEnrichmentGNAQ2.00
50Klippel-trenaunay-weber syndromeEnrichmentGNAQ1.92
51Melanoma, uvealEnrichmentGNAQ1.92
52Nevus, epidermalEnrichmentHRAS1.86
53Thyroid cancer, nonmedullary, 2EnrichmentHRAS1.86
54Noonan syndrome 3EnrichmentHRAS1.86
55BrachydactylyEnrichmentGNAS1.86
56Follicular thyroid carcinomaEnrichmentHRAS1.86
57Melanocytic nevus syndrome, congenitalEnrichmentHRAS1.80
58Spastic paraplegia 4, autosomal dominantEnrichmentGNAS1.80
59Arteriovenous malformationEnrichmentHRAS1.75
60Primary hyperaldosteronismEnrichmentGNAS1.75
61Stroke, ischemicEnrichmentALOX5AP1.70
62Myopathy, x-linked, with excessive autophagyEnrichmentHRAS1.70
63AsthmaEnrichmentALOX51.66
64Lung non-small cell carcinomaEnrichmentHRAS1.66
65Lung cancer susceptibility 3EnrichmentRB11.56
66Noonan syndrome and noonan-related syndromeEnrichmentHRAS1.53
67RhabdomyosarcomaEnrichmentHRAS1.50
68Hypertension, essentialEnrichmentPTGIS1.48
69Noonan syndrome 1EnrichmentHRAS1.35
70Hydrops fetalis, nonimmuneEnrichmentHRAS1.30
71RasopathyEnrichmentHRAS1.30
72Differentiated thyroid carcinomaEnrichmentHRAS1.25
73Non-immune hydrops fetalisEnrichmentHRAS1.22
74Body mass index quantitative trait locus 11EnrichmentGNAS1.02
75Ovarian cancerEnrichmentRB10.74
76Inherited cancer-predisposing syndromeEnrichmentRB10.63

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