Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Valerates	[NCBI]

Gene	Link	Information Gain
ACAT1	[NCBI]	4.74103e-06
AUH	[NCBI]	2.47072e-06
IVD	[NCBI]	2.3959e-06
ACHE	[NCBI]	2.30156e-06
SLC5A6	[NCBI]	2.18852e-06
CA2	[NCBI]	1.97595e-06
SI	[NCBI]	1.91329e-06
F2RL3	[NCBI]	1.811e-06
EGF	[NCBI]	1.81047e-06
BCHE	[NCBI]	1.60966e-06
TNF	[NCBI]	6.75491e-07

OMIM	Link	Information gain
musk, inability to smell	[NCBI]	0.00277021
IVA	[NCBI]	0.00200485
biotinidase deficiency	[NCBI]	0.000388528
3-@methylglutaconic aciduria, type i	[NCBI]	0.000356549
3-@methylcrotonyl-coa carboxylase 1 deficiency	[NCBI]	0.00033754
3-@methylcrotonyl-coa carboxylase 2 deficiency	[NCBI]	0.000244929
PNPLA6	[NCBI]	0.00020242
maple syrup urine disease	[NCBI]	0.000142476
isovaleric acid, inability to smell	[NCBI]	0.00012983
2-@methylbutyryl-coa dehydrogenase deficiency	[NCBI]	0.000122098
alpha-methylacetoacetic aciduria	[NCBI]	8.82474e-05
AUH	[NCBI]	7.77489e-05
holocarboxylase synthetase deficiency	[NCBI]	7.70117e-05
RA	[NCBI]	7.60776e-05
MADD	[NCBI]	6.95831e-05
IVD	[NCBI]	6.24999e-05
MCCC1	[NCBI]	3.54138e-05
MCCC2	[NCBI]	3.46466e-05
ACAT1	[NCBI]	3.11163e-05
3-@hydroxy-3-methylglutaryl-coa lyase deficiency	[NCBI]	2.83108e-05
SI	[NCBI]	1.99521e-05
BCHE	[NCBI]	1.40168e-05
hla-d histocompatibility type	[NCBI]	1.17619e-05
ACHE	[NCBI]	1.02889e-05
EGF	[NCBI]	2.99933e-06
TNF	[NCBI]	5.49247e-08