Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Folic Acid Deficiency	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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