Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Tetrahydrofolates	[NCBI]

Gene	Link	Information Gain
FOLR1	[NCBI]	0.000166277
MTHFR	[NCBI]	1.85641e-05
SLC19A2	[NCBI]	1.65877e-05
DHFR	[NCBI]	1.22663e-05
GNMT	[NCBI]	7.45768e-06
FPGS	[NCBI]	5.88625e-06
ATIC	[NCBI]	3.80086e-06
MTHFD1	[NCBI]	3.39619e-06
SHMT1	[NCBI]	3.32478e-06
RFC1	[NCBI]	3.02559e-06
ABCG2	[NCBI]	1.99151e-06
MTHFD2	[NCBI]	1.92384e-06
SARDH	[NCBI]	1.80289e-06
MAT1A	[NCBI]	1.74483e-06
SHMT2	[NCBI]	1.73209e-06
GGH	[NCBI]	1.598e-06
MTAP	[NCBI]	1.45998e-06
BHMT	[NCBI]	1.4072e-06
CUBN	[NCBI]	1.2177e-06
MTR	[NCBI]	1.16539e-06
SLC4A1	[NCBI]	1.1552e-06
MTRR	[NCBI]	1.13994e-06
PAX3	[NCBI]	1.03373e-06
CYP2E1	[NCBI]	1.01629e-06
PRKACA	[NCBI]	1.0121e-06
NQO1	[NCBI]	9.44403e-07
APC	[NCBI]	7.1728e-07
ACP5	[NCBI]	6.8623e-07
CDK2	[NCBI]	5.8778e-07
CHAT	[NCBI]	5.05422e-07
MBP	[NCBI]	4.64997e-07
TP53	[NCBI]	4.07167e-07
APOE	[NCBI]	3.87119e-07
PCNA	[NCBI]	3.6869e-07
CDKN1A	[NCBI]	3.11794e-07
EGFR	[NCBI]	2.83088e-07

OMIM	Link	Information gain
TYMS	[NCBI]	0.000810293
homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolate reductase activity	[NCBI]	0.000421259
FPGS	[NCBI]	0.000261579
homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cble complementation type	[NCBI]	0.000152301
methionine adenosyltransferase deficiency	[NCBI]	0.000129728
DHFR	[NCBI]	0.000125081
MTR	[NCBI]	0.000117804
GNMT	[NCBI]	7.34708e-05
MTHFR	[NCBI]	6.24871e-05
SLC19A1	[NCBI]	5.50143e-05
FOLR1	[NCBI]	2.46744e-05
MAT1A	[NCBI]	2.36038e-05
GGH	[NCBI]	2.36038e-05
MTAP	[NCBI]	1.73576e-05
homocystinuria	[NCBI]	1.34171e-05
XDH	[NCBI]	3.64598e-06
CHAT	[NCBI]	5.74595e-07
APOE	[NCBI]	3.07841e-07
MBP	[NCBI]	3.06567e-07
EGFR	[NCBI]	1.55581e-07
PCNA	[NCBI]	2.66616e-09