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MeSH keywords -> Related genes, diseases (OMIM)


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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