Prostaglandin synthesis and regulation

Pathway network for the Prostaglandin synthesis and regulation SuperPath

Sources:
  • WikiPathways
  • PharmGKB
  • Reactome

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

Disorders associated with Prostaglandin synthesis and regulation SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Bone diseaseDirect
2Protein-deficiency anemiaDirect
3Waardenburg syndrome, type 4aEnrichmentEDNRB, MITF3.82
4Waardenburg syndromeEnrichmentEDNRB, MITF3.82
5Waardenburg syndrome, type 2eEnrichmentEDNRB, MITF3.67
6Digital clubbing, isolated congenitalEnrichmentHPGD3.53
7Ghosal hematodiaphyseal dysplasiaEnrichmentTBXAS13.53
8Pparg-associated congenital generalized lipodystrophyEnrichmentPPARG3.53
9Hypertension, essentialEnrichmentNOS3, PTGIS3.26
10Carotid intimal medial thickness 1EnrichmentPPARG3.23
11Bleeding disorder, platelet-type, 14EnrichmentTBXAS13.23
12Primary hypertrophic osteoarthropathyEnrichmentHPGD3.23
13Familial partial lipodystrophyEnrichmentPPARG3.23
14Hypertrophic osteoarthropathy, primary, autosomal recessive, 1EnrichmentHPGD3.05
15Currarino syndromeEnrichmentHPGD2.93
16Lipodystrophy, familial partial, type 3EnrichmentPPARG2.93
17Leptin deficiency or dysfunctionEnrichmentPPARG2.93
18Congenital generalized lipodystrophyEnrichmentPPARG2.93
19Pyloric stenosis, infantile hypertrophic, 1EnrichmentNOS12.69
20Asthma-related traits 1EnrichmentPTGDR2.69
21Polysubstance abuseEnrichmentFAAH2.69
22Bleeding disorder, platelet-type, 13EnrichmentTBXA2R2.69
23Cytosolic phospholipase-a2 alpha deficiency associated bleeding disorderEnrichmentPLA2G4A2.69
24Gastrointestinal ulceration, recurrent, with dysfunctional plateletsEnrichmentPLA2G4A2.69
25Bleeding diathesis due to thromboxane synthesis deficiencyEnrichmentTBXA2R2.69
26Cryptogenic multifocal ulcerous stenosing enteritisEnrichmentPLA2G4A2.69
27Apparent mineralocorticoid excessEnrichmentHSD11B22.49
28Heterochromia iridisEnrichmentMITF2.49
29Tietz albinism-deafness syndromeEnrichmentMITF2.49
30Mandibulofacial dysostosis with alopeciaEnrichmentEDNRA2.49
31Adrenal insufficiency, congenital, with 46,xy sex reversal, partial or completeEnrichmentCYP11A12.49
32Auriculocondylar syndrome 3EnrichmentEDN12.49
3346,xy sex reversal 10EnrichmentSOX92.49
3446,xx sex reversal 2EnrichmentSOX92.49
35Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafnessEnrichmentMITF2.49
36Question mark ears, isolatedEnrichmentEDN12.49
37Inherited isolated adrenal insufficiency due to partial cyp11a1 deficiencyEnrichmentCYP11A12.49
38GliosarcomaEnrichmentPPARG2.33
39Giant cell glioblastomaEnrichmentPPARG2.30
40Asthma, nasal polyps, and aspirin intoleranceEnrichmentPTGER22.21
41Campomelic dysplasiaEnrichmentSOX92.19
42Aganglionosis, total intestinalEnrichmentEDNRB2.19
43Abcd syndromeEnrichmentEDNRB2.19
44Melanoma, cutaneous malignant 8EnrichmentMITF2.19
45Cortisone reductase deficiency 2EnrichmentHSD11B12.19
46Cortisone reductase deficiencyEnrichmentHSD11B12.19
47Papillary renal cell carcinomaEnrichmentMITF2.19
48Cic-rearranged sarcomaEnrichmentAKR1C22.19
49Campomelic dysplasia and related disordersEnrichmentSOX92.19
50Idiopathic achalasiaEnrichmentNOS12.08
51Differentiated thyroid carcinomaEnrichmentPPARG2.07
52Waardenburg syndrome, type 2aEnrichmentMITF2.01
53Hirschsprung disease 2EnrichmentEDNRB2.01
5446,xx sex reversal 1EnrichmentSOX92.01
5546,xy sex reversal 8EnrichmentAKR1C22.01
56Alzheimer disease 2EnrichmentNOS31.99
57Pre-eclampsiaEnrichmentNOS31.99
58Type 2 diabetes mellitusEnrichmentPPARG1.91
59Auriculocondylar syndrome 1EnrichmentEDN11.89
60Pregnancy loss, recurrent 3EnrichmentANXA51.89
61Clear cell papillary renal cell carcinomaEnrichmentMITF1.89
62Body mass index quantitative trait locus 11EnrichmentPPARG1.83
63Nonsyndromic 46,xx testicular disorders/differences of sex developmentEnrichmentSOX91.79
64Developmental dysplasia of the hip 1EnrichmentAKR1C11.71
65Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiencyEnrichmentCYP11A11.71
66Pierre robin syndromeEnrichmentSOX91.71
6721-hydroxylase-deficient congenital adrenal hyperplasiaEnrichmentCYP11A11.71
68Stroke, ischemicEnrichmentNOS31.69
69Familial colorectal cancerEnrichmentPLA2G2A1.69
70Waardenburg syndrome, type 1EnrichmentMITF1.65
71Colorectal cancerEnrichmentPPARG1.59
72Rare genetic deafnessEnrichmentEDNRB, MITF1.57
73MelanomaEnrichmentMITF1.50
74Alzheimer disease, familial, 1EnrichmentNOS31.46
7546,xy complete gonadal dysgenesisEnrichmentSOX91.45
76Lipoid congenital adrenal hyperplasiaEnrichmentCYP11A11.35
7746,xy partial gonadal dysgenesisEnrichmentSOX91.35
78MalariaEnrichmentNOS21.33
79Melanoma, cutaneous malignant 1EnrichmentMITF1.27
80Ear malformationEnrichmentMITF1.12
81Hirschsprung disease 1EnrichmentEDNRB1.05
82Cystic fibrosisEnrichmentEDNRA1.01
83Connective tissue diseaseEnrichmentSOX91.01
84Non-syndromic genetic deafnessEnrichmentMITF0.96
85Primary ovarian insufficiencyEnrichmentNOS30.94
86Nonsyndromic hearing lossEnrichmentMITF0.89
87Rare autosomal dominant non-syndromic sensorineural deafness type dfnaEnrichmentMITF0.81
88Hereditary breast ovarian cancer syndromeEnrichmentMITF0.79
89Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentPPARGC1A0.76
90Deafness, autosomal recessiveEnrichmentEDNRB0.73
91Autosomal recessive nonsyndromic deafnessEnrichmentEDNRB0.73
92Rare autosomal recessive non-syndromic sensorineural deafness type dfnbEnrichmentEDNRB0.60
93Inherited cancer-predisposing syndromeEnrichmentMITF0.46

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