triacylglycerol biosynthesis

No Pathway Network information available for triacylglycerol biosynthesis

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

Disorders associated with triacylglycerol biosynthesis SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Rhizomelic chondrodysplasia punctataEnrichmentAGPS, GNPAT4.75
2Rhizomelic chondrodysplasia punctata, type 2EnrichmentGNPAT2.75
3Hepatic lipase deficiencyEnrichmentLIPC2.75
4Hypertriglyceridemia, transient infantileEnrichmentGPD12.75
5High density lipoprotein cholesterol level quantitative trait locus 12EnrichmentLIPC2.75
6Rhizomelic chondrodysplasia punctata, type 3EnrichmentAGPS2.75
7Lipodystrophy, congenital generalized, type 1EnrichmentAGPAT22.75
8Autosomal dominant charcot-marie-tooth disease type 2 due to dgat2 mutationEnrichmentDGAT22.75
9Hyperlipidemia due to hepatic triglyceride lipase deficiencyEnrichmentLIPC2.75
10Primary triglyceride deposit cardiomyovasculopathyEnrichmentPNPLA22.75
11Intellectual developmental disorder, autosomal recessive 57EnrichmentMBOAT72.70
12Hyperlipoproteinemia, type iEnrichmentLPL2.45
13Glycerol kinase deficiencyEnrichmentGK2.45
14Neutral lipid storage disease with myopathyEnrichmentPNPLA22.45
15Lipase deficiency, combinedEnrichmentLPL2.45
16Familial lipoprotein lipase deficiencyEnrichmentLPL2.45
17Transient infantile hypertriglyceridemia and hepatosteatosisEnrichmentGPD12.45
18Chanarin-dorfman syndromeEnrichmentABHD52.40
19Lipodystrophy, familial partial, type 6EnrichmentLIPE2.28
20Diarrhea 7, protein-losing enteropathy typeEnrichmentDGAT12.15
21Congenital generalized lipodystrophyEnrichmentAGPAT22.15
22Coronary artery anomalyEnrichmentLPL2.15
23Hyperlipidemia, familial combined, 3EnrichmentLPL2.05
24Congenital diarrhea 7 with exudative enteropathyEnrichmentDGAT12.05
25DiarrheaEnrichmentDGAT11.98
26Lipid metabolism disorderEnrichmentLIPC1.98
27Cardiomyopathy, dilated, 1aEnrichmentLPL1.44
28Male infertilityEnrichmentGPAT21.18
29Type 2 diabetes mellitusEnrichmentLIPC1.14
30Autosomal recessive non-syndromic intellectual disabilityEnrichmentMBOAT70.96

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