Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Vitamin B 6	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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