Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Valerates [NCBI]

Gene


 Gene Link Information
Gain		 01
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


 OMIM Link Information
gain		 01
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



Database Center for Life Science