MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Vitamin B 6
[NCBI]
Gene
Gene
Link
Information
Gain
01
MTHFR
[NCBI]
4.54217e-05
CBS
[NCBI]
1.37728e-05
MTRR
[NCBI]
1.36638e-05
MTR
[NCBI]
9.40426e-06
CST3
[NCBI]
6.91901e-06
PDXP
[NCBI]
4.69732e-06
SHMT1
[NCBI]
3.87252e-06
PNPO
[NCBI]
2.17175e-06
MMACHC
[NCBI]
2.12883e-06
SHMT2
[NCBI]
2.00431e-06
TKT
[NCBI]
1.85549e-06
MTHFD1
[NCBI]
1.78124e-06
LOX
[NCBI]
1.57638e-06
OAT
[NCBI]
1.55937e-06
DDC
[NCBI]
1.45537e-06
FOLH1
[NCBI]
1.25676e-06
ALDH2
[NCBI]
1.18495e-06
BRAF
[NCBI]
1.0479e-06
TNFRSF11A
[NCBI]
1.00052e-06
ACP5
[NCBI]
9.53567e-07
MLH1
[NCBI]
8.46676e-07
LIF
[NCBI]
8.29115e-07
IL1RN
[NCBI]
7.7251e-07
NOS3
[NCBI]
7.63581e-07
CAT
[NCBI]
7.55511e-07
VWF
[NCBI]
6.59551e-07
OMIM
OMIM
Link
Information
gain
01
aromatic l-amino acid decarboxylase deficiency
[NCBI]
0.000143901
EPD
[NCBI]
0.000125616
neural tube defects, folate-sensitive
[NCBI]
0.000121336
homocysteinemia
[NCBI]
0.000106571
homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolate reductase activity
[NCBI]
0.000100123
AD
[NCBI]
7.25076e-05
anemia, sideroblastic, x-linked
[NCBI]
6.45076e-05
PDXP
[NCBI]
4.55989e-05
SGPL1
[NCBI]
4.27972e-05
PD
[NCBI]
4.23899e-05
PNPO
[NCBI]
4.09778e-05
TKT
[NCBI]
3.14987e-05
CRC
[NCBI]
2.74238e-05
MMP9
[NCBI]
2.55397e-05
LOX
[NCBI]
2.42557e-05
MTHFR
[NCBI]
2.38677e-05
MTR
[NCBI]
2.37444e-05
homocystinuria
[NCBI]
2.23579e-05
DDC
[NCBI]
2.09997e-05
F3
[NCBI]
8.0051e-06
CAT
[NCBI]
6.93588e-06
RA
[NCBI]
6.94076e-07
Database Center for Life Science