Energy metabolism

No Pathway Network information available for Energy metabolism

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

Disorders associated with Energy metabolism SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Leptin deficiency or dysfunctionEnrichmentPPARG, UCP34.15
2Body mass index quantitative trait locus 11EnrichmentPPARG, UCP2, UCP33.17
3Developmental and epileptic encephalopathy 91EnrichmentPPP3CA2.46
4Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual developmentEnrichmentPPP3CA2.46
5Body mass index quantitative trait locus 4EnrichmentUCP22.46
6Cardiomyopathy, familial hypertrophic, 6EnrichmentPRKAG22.46
7Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired languageEnrichmentMEF2C2.46
8Glycogen storage disease of heart, lethal congenitalEnrichmentPRKAG22.46
9Coronary artery disease, autosomal dominant, 1EnrichmentMEF2A2.46
10Skeletal muscle glycogen content and metabolism quantitative trait locusEnrichmentPRKAG32.46
11Intellectual developmental disorder, autosomal dominant 59EnrichmentCAMK2G2.46
12Pparg-associated congenital generalized lipodystrophyEnrichmentPPARG2.46
135q14.3 microdeletion syndromeEnrichmentMEF2C2.46
14Complete atrioventricular septal defect without ventricular hypoplasiaEnrichmentMEF2C2.46
15Mef2c-related disorderEnrichmentMEF2C2.46
16Hyperinsulinism due to ucp2 deficiencyEnrichmentUCP22.46
17Carotid intimal medial thickness 1EnrichmentPPARG2.16
18Histiocytoma, angiomatoid fibrousEnrichmentCREB12.16
19Menke-hennekam syndrome 2EnrichmentEP3002.16
20Mitochondrial dna depletion syndrome 15EnrichmentTFAM2.16
21Familial partial lipodystrophyEnrichmentPPARG2.16
22Melanoma of soft tissueEnrichmentCREB11.98
23Lipodystrophy, familial partial, type 3EnrichmentPPARG1.86
24Congenital generalized lipodystrophyEnrichmentPPARG1.86
25Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentMEF2C, PPARGC1A1.77
26Rhabdomyosarcoma 2EnrichmentFOXO11.76
27Rubinstein-taybi syndrome 2EnrichmentEP3001.76
28Rubinstein-taybi syndrome 1EnrichmentEP3001.69
29Chromosome 16p13.3 deletion syndrome, proximalEnrichmentEP3001.69
30Charge syndromeEnrichmentEP3001.51
31Rare mitochondrial non-syndromic sensorineural deafnessEnrichmentTFB1M1.47
32Colorectal cancerEnrichmentEP300, PPARG1.44
33Polydactyly, postaxial, type a1EnrichmentEP3001.29
34Rare genetic intellectual disabilityEnrichmentEP3001.29
35Wolff-parkinson-white syndromeEnrichmentPRKAG21.27
36GliosarcomaEnrichmentPPARG1.27
37Giant cell glioblastomaEnrichmentPPARG1.24
38Diffuse large b-cell lymphomaEnrichmentFOXO11.19
39Differentiated thyroid carcinomaEnrichmentPPARG1.02
40Familial hypertrophic cardiomyopathyEnrichmentPRKAG20.97
41Type 2 diabetes mellitusEnrichmentPPARG0.87
42Hypertrophic cardiomyopathyEnrichmentPRKAG20.86
43Autosomal dominant non-syndromic intellectual disabilityEnrichmentPPP3CA0.80
44Myeloma, multipleEnrichmentRXRA0.75
45Undetermined early-onset epileptic encephalopathyEnrichmentPPP3CA0.75
46AutismEnrichmentCAMK2G0.65
47Autism spectrum disorderEnrichmentMEF2C0.50
48MicrocephalyEnrichmentEP3000.46

Loading...
Loading...
Loading...