HIF1A and PPARG regulation of glycolysis

No Pathway Network information available for HIF1A and PPARG regulation of glycolysis

Pathways in the HIF1A and PPARG regulation of glycolysis SuperPath

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

Disorders associated with HIF1A and PPARG regulation of glycolysis SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Stomatin-deficient cryohydrocytosis with neurologic defectsEnrichmentSLC2A13.23
2Triosephosphate isomerase deficiencyEnrichmentTPI13.23
3Hypertriglyceridemia, transient infantileEnrichmentGPD13.23
4Epilepsy, idiopathic generalized 12EnrichmentSLC2A13.23
5Pparg-associated congenital generalized lipodystrophyEnrichmentPPARG3.23
6Epilepsy with myoclonic absencesEnrichmentSLC2A13.23
7Hereditary cryohydrocytosis with reduced stomatinEnrichmentSLC2A13.23
8Fanconi-bickel syndromeEnrichmentLDHA2.93
9Dystonia 9EnrichmentSLC2A12.93
10Carotid intimal medial thickness 1EnrichmentPPARG2.93
11Glut1 deficiency syndrome 1EnrichmentSLC2A12.93
12Microcephaly 21, primary, autosomal recessiveEnrichmentGAPDH2.93
13Glucose transporter type 1 deficiency syndromeEnrichmentSLC2A12.93
14Familial partial lipodystrophyEnrichmentPPARG2.93
15Transient infantile hypertriglyceridemia and hepatosteatosisEnrichmentGPD12.93
16Glut1 deficiency syndrome 2EnrichmentSLC2A12.75
17Chromosome 17q23.1-q23.2 deletion syndromeEnrichmentSLC2A12.75
18EnchondromatosisEnrichmentHIF1A2.75
19Lipodystrophy, familial partial, type 3EnrichmentPPARG2.63
20Leptin deficiency or dysfunctionEnrichmentPPARG2.63
21Congenital generalized lipodystrophyEnrichmentPPARG2.63
22Enchondromatosis, multiple, ollier typeEnrichmentHIF1A2.53
23Multiple enchondromatosis, maffucci typeEnrichmentHIF1A2.38
24Paroxysmal dystoniaEnrichmentSLC2A12.38
25Alternating hemiplegia of childhoodEnrichmentSLC2A12.33
26Myoclonic-atonic epilepsyEnrichmentSLC2A12.28
27GliosarcomaEnrichmentPPARG2.03
28Giant cell glioblastomaEnrichmentPPARG2.00
29Developmental and epileptic encephalopathy 1EnrichmentSLC2A11.83
30StrabismusEnrichmentSLC2A11.80
31Differentiated thyroid carcinomaEnrichmentPPARG1.77
32EpilepsyEnrichmentSLC2A11.63
33Benign epilepsy with centrotemporal spikesEnrichmentSLC2A11.62
34Type 2 diabetes mellitusEnrichmentPPARG1.61
35Centralopathic epilepsyEnrichmentSLC2A11.60
36West syndromeEnrichmentSLC2A11.59
37Body mass index quantitative trait locus 11EnrichmentPPARG1.54
38Colorectal cancerEnrichmentPPARG1.30
39MicrocephalyEnrichmentSLC2A11.15

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