PPAR signaling pathway

Pathway network for the PPAR signaling pathway SuperPath

Sources:
  • WikiPathways

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

Disorders associated with PPAR signaling pathway SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Phosphoenolpyruvate carboxykinase deficiencyEnrichmentPCK1, PCK24.13
2Coronary artery anomalyEnrichmentAPOC3, LPL3.83
3Intellectual developmental disorder, x-linked 63EnrichmentACSL42.88
4Coronary heart disease 7EnrichmentCD362.88
5Diarrhea 13EnrichmentACSL52.88
6Platelet glycoprotein iv deficiencyEnrichmentCD362.88
7Ichthyosis prematurity syndromeEnrichmentSLC27A42.88
8Phosphoenolpyruvate carboxykinase deficiency, cytosolicEnrichmentPCK12.30
9Acyl-coa dehydrogenase, medium-chain, deficiency ofEnrichmentACADM2.30
10Cerebrotendinous xanthomatosisEnrichmentCYP27A12.30
11Fanconi renotubular syndrome 3EnrichmentEHHADH2.30
12Peroxisomal acyl-coa oxidase deficiencyEnrichmentACOX12.30
13Bile acid synthesis defect, congenital, 6EnrichmentACOX22.30
14Mitchell syndromeEnrichmentACOX12.30
15Familial apolipoprotein a5 deficiencyEnrichmentAPOA52.30
16Glycerol quantitative trait locusEnrichmentAQP72.30
17Apolipoprotein c-iii deficiencyEnrichmentAPOC32.30
18Plasma triglyceride level quantitative trait locusEnrichmentANGPTL42.30
19Leukoencephalopathy with dystonia and motor neuropathyEnrichmentSCP22.30
20Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiencyEnrichmentCYP7A12.30
21Pparg-associated congenital generalized lipodystrophyEnrichmentPPARG2.30
22Medium-chain acyl-coenzyme a dehydrogenase deficiencyEnrichmentACADM2.30
23Aapoaii amyloidosisEnrichmentAPOA22.30
24Amme complexEnrichmentACSL42.28
25Blood platelet diseaseEnrichmentCD362.28
26Cerebral malariaEnrichmentCD362.28
27Hyperlipoproteinemia, type vEnrichmentAPOA52.00
28Hyperlipoproteinemia, type iEnrichmentLPL2.00
29Phosphoenolpyruvate carboxykinase deficiency, mitochondrialEnrichmentPCK22.00
30Carnitine palmitoyltransferase ii deficiency, infantileEnrichmentCPT22.00
31Carotid intimal medial thickness 1EnrichmentPPARG2.00
32Carnitine palmitoyltransferase ii deficiency, lethal neonatalEnrichmentCPT22.00
33Lipase deficiency, combinedEnrichmentLPL2.00
34Carnitine palmitoyltransferase i deficiencyEnrichmentCPT1A2.00
35Carnitine palmitoyltransferase ii deficiency, myopathic, stress-inducedEnrichmentCPT22.00
36Encephalopathy, acute, infection-induced 4EnrichmentCPT22.00
37Spastic paraplegia 73, autosomal dominantEnrichmentCPT1C2.00
383-hydroxy-3-methylglutaryl-coa synthase-2 deficiencyEnrichmentHMGCS22.00
39Recessive dystrophic epidermolysis bullosaEnrichmentMMP12.00
40Familial lipoprotein lipase deficiencyEnrichmentLPL2.00
41Hypoalphalipoproteinemia, primary, 2, intermediateEnrichmentAPOA12.00
42Amyloidosis, hereditary systemic 3EnrichmentAPOA12.00
43Familial partial lipodystrophyEnrichmentPPARG2.00
44Acute necrotizing encephalopathy of childhoodEnrichmentCPT22.00
45Stroke, ischemicEnrichmentACSL41.88
46Hyperalphalipoproteinemia 1EnrichmentAPOC31.82
47D-bifunctional protein deficiencyEnrichmentEHHADH1.82
48Adiponectin deficiencyEnrichmentADIPOQ1.82
49Lipodystrophy, familial partial, type 4EnrichmentPLIN11.82
50Hypoalphalipoproteinemia, primary, 2EnrichmentAPOA11.82
51Spastic paraplegia 50, autosomal recessiveEnrichmentAPOA11.82
52Autosomal recessive congenital ichthyosisEnrichmentSLC27A41.70
53Hypertriglyceridemia 1EnrichmentAPOA51.70
54Hypoalphalipoproteinemia, primary, 1EnrichmentAPOA11.70
55Lipodystrophy, familial partial, type 3EnrichmentPPARG1.70
56Leptin deficiency or dysfunctionEnrichmentPPARG1.70
57Congenital generalized lipodystrophyEnrichmentPPARG1.70
58Hydrocephalus, congenital, 2, with or without brain or eye anomaliesEnrichmentACADM1.70
59Primary fanconi renotubular syndromeEnrichmentEHHADH1.70
60Hyperlipidemia, familial combined, 3EnrichmentLPL1.61
61Amyloidosis, hereditary systemic 2EnrichmentAPOA11.61
62Body mass index quantitative trait locus 11EnrichmentAQP7, PPARG1.59
63MalariaEnrichmentCD361.52
64Non-syndromic x-linked intellectual disabilityEnrichmentACSL41.33
65Hypercholesterolemia, familial, 1EnrichmentAPOA21.20
66Multiple sclerosisEnrichmentNR1H31.17
67Familial hypercholesterolemiaEnrichmentAPOA21.14
68GliosarcomaEnrichmentPPARG1.11
69Giant cell glioblastomaEnrichmentPPARG1.09
70Cardiomyopathy, dilated, 1aEnrichmentLPL1.00
71Myocardial infarctionEnrichmentOLR10.98
72Differentiated thyroid carcinomaEnrichmentPPARG0.87
73Type 2 diabetes mellitusEnrichmentPPARG0.72
74Myeloma, multipleEnrichmentRXRA0.61
75Colorectal cancerEnrichmentPPARG0.45
76Congenital nervous system abnormalityEnrichmentCPT20.38
77Nervous system diseaseEnrichmentCPT20.38

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