MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Folic Acid Deficiency
[NCBI]
Gene
Gene
Link
Information
Gain
01
MIR122
[NCBI]
0.000355204
FOLR1
[NCBI]
0.000283617
MTHFR
[NCBI]
0.00022589
RFC1
[NCBI]
3.80391e-05
MTRR
[NCBI]
3.11959e-05
TYMS
[NCBI]
2.09835e-05
GNMT
[NCBI]
2.0135e-05
BHMT
[NCBI]
1.85221e-05
SHMT1
[NCBI]
1.79328e-05
SLC19A1
[NCBI]
1.7278e-05
MTR
[NCBI]
1.30598e-05
APOE
[NCBI]
1.16129e-05
F2RL2
[NCBI]
1.05519e-05
TCN1
[NCBI]
9.67479e-06
FPGS
[NCBI]
9.19857e-06
MBD1
[NCBI]
8.82646e-06
MTHFD1
[NCBI]
7.74736e-06
MS
[NCBI]
7.68417e-06
CST3
[NCBI]
7.57889e-06
IRF6
[NCBI]
6.76333e-06
SLC19A2
[NCBI]
6.34637e-06
NOS3
[NCBI]
5.7884e-06
DCC
[NCBI]
5.5307e-06
CBS
[NCBI]
5.47197e-06
GPX1
[NCBI]
5.16704e-06
PLK1
[NCBI]
5.13848e-06
TFRC
[NCBI]
4.79846e-06
FOLH1
[NCBI]
4.41068e-06
ABCG2
[NCBI]
3.96421e-06
ALB
[NCBI]
3.78663e-06
MECP2
[NCBI]
3.68356e-06
IGF1
[NCBI]
3.57249e-06
COMT
[NCBI]
3.20532e-06
BACE1
[NCBI]
2.87337e-06
ACHE
[NCBI]
1.94984e-06
TGFB1
[NCBI]
1.27508e-06
VWF
[NCBI]
1.19301e-06
EPO
[NCBI]
1.13056e-06
AFP
[NCBI]
1.08254e-06
CDKN1A
[NCBI]
6.38766e-07
OMIM
OMIM
Link
Information
gain
01
folic acid, transport defect involving
[NCBI]
0.00695955
formiminotransferase deficiency
[NCBI]
0.000294082
CRC
[NCBI]
0.000273883
GNMT
[NCBI]
0.00011537
fibromatosis, gingival, with hypertrichosis
[NCBI]
8.66409e-05
APOE
[NCBI]
7.40317e-05
TYMS
[NCBI]
7.13296e-05
homocysteinemia
[NCBI]
5.95137e-05
MTHFD1
[NCBI]
5.86684e-05
CDC25C
[NCBI]
5.86684e-05
CD
[NCBI]
4.37935e-05
DCC
[NCBI]
4.19402e-05
PLK1
[NCBI]
3.64689e-05
KSS
[NCBI]
3.35107e-05
SERPINA6
[NCBI]
3.27902e-05
fragile x mental retardation syndrome
[NCBI]
3.23441e-05
homocystinuria
[NCBI]
3.23232e-05
CPI
[NCBI]
2.91693e-05
COMT
[NCBI]
2.03403e-05
ALB
[NCBI]
2.02896e-05
DHFR
[NCBI]
1.7583e-05
F3
[NCBI]
1.11778e-05
RA
[NCBI]
1.10339e-05
lymphoma, non-hodgkin, familial
[NCBI]
1.01232e-05
ACHE
[NCBI]
9.19037e-06
SLE
[NCBI]
6.77576e-06
EPO
[NCBI]
4.8736e-06
AFP
[NCBI]
4.65406e-06
AD
[NCBI]
4.88936e-07
Database Center for Life Science