MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
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