Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Hydroxy Acids	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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