Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Ketosis [NCBI]


Gene


Gene Link Information
Gain
01
OXCT1 [NCBI] 3.25683e-05
SLC2A1 [NCBI] 2.52859e-05
OXCT2 [NCBI] 2.36081e-05
FGF21 [NCBI] 1.36815e-05
AMT [NCBI] 1.27007e-05
NDUFV1 [NCBI] 1.27007e-05
EBI3 [NCBI] 1.19797e-05
ACAT1 [NCBI] 1.19797e-05
GLDC [NCBI] 1.18843e-05
PCCB [NCBI] 1.17939e-05
SLC25A13 [NCBI] 1.03777e-05
IL12A [NCBI] 9.05023e-06
PPARA [NCBI] 8.78731e-06
PTPRN [NCBI] 7.86756e-06
TF [NCBI] 6.5212e-06
APOB [NCBI] 5.79164e-06
FASLG [NCBI] 3.7062e-06
PTH [NCBI] 2.79151e-06




OMIM


OMIM Link Information
gain
01
IDDM [NCBI] 0.000674807
GCE [NCBI] 0.000273254
OXCT1 [NCBI] 0.000243442
succinyl-coa:3-oxoacid coa transferase deficiency [NCBI] 0.00020285
IVA [NCBI] 0.000168437
PCCA [NCBI] 0.000130109
glycogen storage disease 0, liver [NCBI] 9.48731e-05
glucose transport defect, blood-brain barrier [NCBI] 7.97839e-05
GPD1 [NCBI] 7.77884e-05
HSS [NCBI] 7.40678e-05
acyl-coa dehydrogenase, medium-chain, deficiency of [NCBI] 7.40678e-05
LCAT [NCBI] 6.96633e-05
MADD [NCBI] 6.93382e-05
GPD2 [NCBI] 6.9211e-05
myoclonic epilepsy of lafora [NCBI] 6.88341e-05
pyruvate decarboxylase deficiency [NCBI] 6.41361e-05
AMT [NCBI] 5.92612e-05
SLC2A1 [NCBI] 5.37769e-05
transcobalamin ii deficiency [NCBI] 5.06988e-05
ADCYAP1 [NCBI] 3.3178e-05
TS [NCBI] 2.48381e-05
TF [NCBI] 2.30056e-05
APOB [NCBI] 1.91856e-05
PTH [NCBI] 3.29613e-06




Database Center for Life Science