Transcriptional regulation of brown and beige adipocyte differentiation

No Pathway Network information available for Transcriptional regulation of brown and beige adipocyte differentiation

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

Disorders associated with Transcriptional regulation of brown and beige adipocyte differentiation SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Spermatogenic failure, x-linked, 9EnrichmentRBBP72.66
2Gand syndromeEnrichmentGATAD2B2.66
3Developmental and epileptic encephalopathy 54EnrichmentHNRNPU2.66
4Left ventricular noncompaction 8EnrichmentPRDM162.66
5Nephronophthisis 14EnrichmentZNF4232.66
6Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndromeEnrichmentGATAD2B2.66
7Pparg-associated congenital generalized lipodystrophyEnrichmentPPARG2.66
8Heritable thoracic aortic diseaseEnrichmentSMAD42.66
91q44 microdeletion syndromeEnrichmentHNRNPU2.66
10Myhre syndromeEnrichmentSMAD42.35
11Carotid intimal medial thickness 1EnrichmentPPARG2.35
12Juvenile polyposis/hereditary hemorrhagic telangiectasia syndromeEnrichmentSMAD42.35
13Sifrim-hitz-weiss syndromeEnrichmentCHD42.35
14Snijders blok-campeau syndromeEnrichmentCHD32.35
15Familial partial lipodystrophyEnrichmentPPARG2.35
16Juvenile polyposis syndromeEnrichmentSMAD42.18
17Lipodystrophy, familial partial, type 3EnrichmentPPARG2.05
18Leptin deficiency or dysfunctionEnrichmentPPARG2.05
19Congenital generalized lipodystrophyEnrichmentPPARG2.05
20Ventricular septal defect 1EnrichmentBMP71.96
21Congenital heart defects, multiple types, 4EnrichmentBMP71.96
22Generalized juvenile polyposis/juvenile polyposis coliEnrichmentSMAD41.96
23Arima syndromeEnrichmentZNF4231.81
24Gallbladder cancerEnrichmentSMAD41.81
25Hereditary hemorrhagic telangiectasiaEnrichmentSMAD41.81
26Colorectal cancerEnrichmentPPARG, SMAD41.80
27Infantile nephronophthisisEnrichmentZNF4231.76
28Chromosome 1p36 deletion syndromeEnrichmentPRDM161.55
29GliosarcomaEnrichmentPPARG1.46
30Giant cell glioblastomaEnrichmentPPARG1.43
31Pancreatic cancerEnrichmentSMAD41.27
32Differentiated thyroid carcinomaEnrichmentPPARG1.21
33Left ventricular noncompactionEnrichmentPRDM161.13
34Type 2 diabetes mellitusEnrichmentPPARG1.05
35Gastric cancerEnrichmentSMAD41.04
36Familial thoracic aortic aneurysm and aortic dissectionEnrichmentSMAD41.03
37ThrombocytopeniaEnrichmentSMAD41.00
38Body mass index quantitative trait locus 11EnrichmentPPARG0.98
39Familial isolated dilated cardiomyopathyEnrichmentPRDM160.95
40Myeloma, multipleEnrichmentRXRA0.93
41Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentPPARGC1A0.92
42Inherited cancer-predisposing syndromeEnrichmentSMAD40.59

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