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MeSH keywords -> Related genes, diseases (OMIM)


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01 Hydroxy Acids [NCBI]


Gene


Gene Link Information
Gain
01
CYP2A [NCBI] 0.000207504
KCNJ8 [NCBI] 3.7445e-05
LDHD [NCBI] 6.34996e-06
CS [NCBI] 3.03478e-06
L2HGDH [NCBI] 2.20181e-06
CYP2A13 [NCBI] 1.9018e-06
ADORA1 [NCBI] 1.86797e-06
ACADM [NCBI] 1.86797e-06
ABCC4 [NCBI] 1.68392e-06
NR1I3 [NCBI] 1.36421e-06
ALDH2 [NCBI] 1.27672e-06
ITGB3 [NCBI] 1.2431e-06
SHBG [NCBI] 1.08653e-06
ACP5 [NCBI] 1.04486e-06
BCL2L1 [NCBI] 8.84818e-07
NOS3 [NCBI] 8.54009e-07
AKT1 [NCBI] 7.79765e-07
MPO [NCBI] 7.70266e-07
PTGS2 [NCBI] 6.19385e-07
EGFR [NCBI] 6.18047e-07
TNF [NCBI] 4.04323e-07




OMIM


OMIM Link Information
gain
01
3-@methylcrotonyl-coa carboxylase 1 deficiency [NCBI] 0.000251628
holocarboxylase synthetase deficiency [NCBI] 0.000234066
biotinidase deficiency [NCBI] 0.00020734
ketoadipicaciduria [NCBI] 0.000196291
3-@hydroxy-3-methylglutaryl-coa synthase 2, mitochondrial, deficiency of [NCBI] 0.000152784
l-2-hydroxyglutaric aciduria [NCBI] 0.000122247
acyl-coa dehydrogenase, medium-chain, deficiency of [NCBI] 9.5008e-05
adrenoleukodystrophy, autosomal neonatal form [NCBI] 8.82258e-05
ZS [NCBI] 6.95213e-05
ACADM [NCBI] 5.02856e-05
L2HGDH [NCBI] 4.09714e-05
HMGCS2 [NCBI] 3.82295e-05
FMF [NCBI] 3.6188e-05
tyrosine transaminase deficiency [NCBI] 3.31118e-05
3-@hydroxy-3-methylglutaryl-coa lyase deficiency [NCBI] 3.18902e-05
ABCC2 [NCBI] 2.38406e-05
SHBG [NCBI] 1.19392e-05
MPO [NCBI] 6.72628e-06
EGFR [NCBI] 4.7912e-06
TNF [NCBI] 1.3831e-06




Database Center for Life Science