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MeSH keywords -> Related genes, diseases (OMIM)


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01 Pyridoxine [NCBI]


Gene


Gene Link Information
Gain
01
HFM [NCBI] 0.000202139
MS [NCBI] 2.40236e-05
ALDH7A1 [NCBI] 2.32084e-05
CBS [NCBI] 2.19053e-05
ALAS2 [NCBI] 1.06674e-05
OAT [NCBI] 9.49714e-06
AGXT2L1 [NCBI] 8.74615e-06
MTHFR [NCBI] 7.59103e-06
TAT [NCBI] 6.22397e-06
SHMT2 [NCBI] 4.19109e-06
PRL [NCBI] 3.01372e-06
KYNU [NCBI] 2.12056e-06
PNPO [NCBI] 2.06941e-06
CST3 [NCBI] 2.05714e-06
PDXK [NCBI] 1.88981e-06
AGXT [NCBI] 1.72607e-06
NAGS [NCBI] 1.64835e-06
SHMT1 [NCBI] 1.64357e-06
BHMT [NCBI] 1.57692e-06
ALDH5A1 [NCBI] 1.54564e-06
ALPL [NCBI] 1.52666e-06
VWF [NCBI] 1.48425e-06
EPO [NCBI] 1.4477e-06
DDC [NCBI] 1.35322e-06
ACHE [NCBI] 1.33441e-06
UMOD [NCBI] 9.69366e-07
SERPINE1 [NCBI] 9.58024e-07
ALB [NCBI] 9.56952e-07
COMT [NCBI] 8.40842e-07
CTSL1 [NCBI] 8.06055e-07
HFE [NCBI] 8.02683e-07
TNF [NCBI] 7.95499e-07
NOS3 [NCBI] 6.63924e-07
NOS2 [NCBI] 6.51768e-07
AFP [NCBI] 6.05324e-07




OMIM


OMIM Link Information
gain
01
hydroxykynureninuria [NCBI] 0.00565397
CTS1 [NCBI] 0.00535502
EPD [NCBI] 0.0016589
candidiasis, familial chronic mucocutaneous, autosomal recessive [NCBI] 0.00154489
candidiasis, familial chronic mucocutaneous, autosomal dominant [NCBI] 0.00132303
MCDU [NCBI] 0.00124792
HFM [NCBI] 0.00113239
iminoglycinuria [NCBI] 0.00108597
homocystinuria [NCBI] 0.000795967
cystathioninuria [NCBI] 0.000786247
hyperoxaluria, primary, type i [NCBI] 0.000647821
anemia, sideroblastic, x-linked [NCBI] 0.000443609
aromatic l-amino acid decarboxylase deficiency [NCBI] 0.000390626
ornithine aminotransferase deficiency [NCBI] 0.00020092
sideroblastic anemia, autosomal [NCBI] 0.000165967
convulsive disorder, familial, with prenatal or early onset [NCBI] 0.000165967
homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolate reductase activity [NCBI] 0.000146663
PDXK [NCBI] 0.000139325
hyper-beta-alaninemia [NCBI] 0.000134391
myoclonic epilepsy, neonatal, with suppression-burst pattern [NCBI] 0.000109013
hyperoxaluria, primary, type ii [NCBI] 0.000100639
bladder cancer [NCBI] 8.5814e-05
COH1 [NCBI] 8.40748e-05
hypophosphatasia, adult type [NCBI] 7.95466e-05
SLE [NCBI] 7.70472e-05
TRMA [NCBI] 7.69697e-05
hyperekplexia, hereditary [NCBI] 7.57852e-05
ALDH7A1 [NCBI] 7.26909e-05
GCE [NCBI] 6.8074e-05
glycogen storage disease v [NCBI] 6.43442e-05
homocysteinemia [NCBI] 6.36691e-05
CPI [NCBI] 4.38899e-05
LCT [NCBI] 3.56175e-05
SGPL1 [NCBI] 3.35098e-05
RA [NCBI] 3.02829e-05
ABP1 [NCBI] 2.60384e-05
GAD1 [NCBI] 2.4461e-05
AGXT [NCBI] 2.33905e-05
tay-sachs disease, ab variant [NCBI] 2.17383e-05
ALPL [NCBI] 1.99499e-05
MTHFR [NCBI] 1.46843e-05
DDC [NCBI] 1.18928e-05
AGER [NCBI] 1.09694e-05
PRL [NCBI] 5.12836e-06
ALB [NCBI] 4.7064e-06
COMT [NCBI] 3.78876e-06
EPO [NCBI] 2.03262e-06
TNF [NCBI] 1.3961e-06
ACHE [NCBI] 9.73428e-07
NPPA [NCBI] 6.47192e-07
AFP [NCBI] 1.30111e-07




Database Center for Life Science