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MeSH keywords -> Related genes, diseases (OMIM)


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01 Hydroxybutyrates [NCBI]

Gene


 Gene Link Information
Gain		 01
MS [NCBI] 5.5892e-05
ALDH5A1 [NCBI] 5.34133e-05
OXCT2 [NCBI] 2.1099e-05
LPL [NCBI] 8.01517e-06
ACAT1 [NCBI] 5.91714e-06
ADHFE1 [NCBI] 4.92119e-06
PTGS2 [NCBI] 3.10347e-06
GIP [NCBI] 2.39389e-06
SLC2A1 [NCBI] 2.1931e-06
HIBADH [NCBI] 2.16342e-06
BDH1 [NCBI] 2.07331e-06
D2HGDH [NCBI] 2.04895e-06
DHODH [NCBI] 1.96907e-06
SLC16A3 [NCBI] 1.95234e-06
SLC16A7 [NCBI] 1.84658e-06
PDK2 [NCBI] 1.83588e-06
SLC5A8 [NCBI] 1.78799e-06
PDK4 [NCBI] 1.76289e-06
SLC16A4 [NCBI] 1.68102e-06
EGF [NCBI] 1.54781e-06
PC [NCBI] 1.39337e-06
CAD [NCBI] 1.32035e-06
C3 [NCBI] 1.31286e-06
ACHE [NCBI] 1.29456e-06
SCP2 [NCBI] 1.17432e-06
HCFC1 [NCBI] 1.12193e-06
CS [NCBI] 1.11413e-06
POU2F1 [NCBI] 1.10117e-06
MMP13 [NCBI] 1.05045e-06
SLC2A4 [NCBI] 9.61354e-07
TNF [NCBI] 7.58214e-07
IL6 [NCBI] 7.14744e-07
IL1RN [NCBI] 6.52955e-07
MPO [NCBI] 5.62297e-07
AVP [NCBI] 5.3415e-07
VIP [NCBI] 5.34078e-07
CCK [NCBI] 5.12721e-07
PCNA [NCBI] 5.06416e-07
TH [NCBI] 4.94968e-07
PRL [NCBI] 3.77121e-07



OMIM


 OMIM Link Information
gain		 01
3-@hydroxyisobutyric aciduria [NCBI] 0.00541205
methionine malabsorption syndrome [NCBI] 0.00179377
carnitine deficiency, myopathic [NCBI] 0.00141752
succinic semialdehyde dehydrogenase deficiency [NCBI] 0.00141432
alpha-methylacetoacetic aciduria [NCBI] 0.000484201
succinyl-coa:3-oxoacid coa transferase deficiency [NCBI] 0.000220078
lactic acidosis, chronic adult form [NCBI] 0.00017125
LS [NCBI] 0.000128232
ALDH5A1 [NCBI] 0.000114317
hydroxyacyl-coa dehydrogenase ii deficiency [NCBI] 0.000105902
donohue syndrome [NCBI] 8.47774e-05
acyl-coa dehydrogenase, short-chain, deficiency of [NCBI] 8.2194e-05
LPL [NCBI] 8.1306e-05
pyruvate carboxylase deficiency [NCBI] 8.10063e-05
ADHFE1 [NCBI] 8.01139e-05
acyl-coa dehydrogenase, medium-chain, deficiency of [NCBI] 7.02231e-05
mitochondrial complex iv deficiency [NCBI] 6.75477e-05
ACAT1 [NCBI] 6.34278e-05
pyruvate decarboxylase deficiency [NCBI] 6.30142e-05
RA [NCBI] 4.37472e-05
OXCT1 [NCBI] 3.29367e-05
PCCA [NCBI] 2.61629e-05
3-@hydroxy-3-methylglutaryl-coa lyase deficiency [NCBI] 2.49441e-05
GIP [NCBI] 2.4593e-05
SLC16A1 [NCBI] 2.16448e-05
DAO [NCBI] 2.02188e-05
PC [NCBI] 1.63994e-05
IL6 [NCBI] 1.4225e-05
GPI [NCBI] 1.08418e-05
hla-d histocompatibility type [NCBI] 8.58727e-06
ACHE [NCBI] 5.01414e-06
EGF [NCBI] 2.62163e-06
MPO [NCBI] 1.45045e-06
VIP [NCBI] 1.04962e-06
PCNA [NCBI] 8.34258e-07
CCK [NCBI] 8.31621e-07
TH [NCBI] 6.64353e-07
AVP [NCBI] 5.7984e-07
TNF [NCBI] 2.4702e-07
PRL [NCBI] 1.01243e-08



Database Center for Life Science