Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Mitomycins	[NCBI]

Gene	Link	Information Gain
MS	[NCBI]	0.000111788
TNF	[NCBI]	6.79563e-06
AFP	[NCBI]	6.39028e-06
DNASE2B	[NCBI]	3.38086e-06
DHFR	[NCBI]	2.38989e-06
AHRR	[NCBI]	2.04227e-06
FASLG	[NCBI]	1.95445e-06
EPO	[NCBI]	1.91264e-06
ERCC3	[NCBI]	1.76654e-06
ERCC4	[NCBI]	1.62995e-06
XDH	[NCBI]	1.55946e-06
CDKN1C	[NCBI]	1.48786e-06
ARNT	[NCBI]	1.37974e-06
CTNNA1	[NCBI]	1.30637e-06
CDH1	[NCBI]	1.23492e-06
PGR	[NCBI]	1.21364e-06
IL2	[NCBI]	1.154e-06
AHR	[NCBI]	1.09384e-06
GSTP1	[NCBI]	1.08305e-06
CD38	[NCBI]	1.0743e-06
CTNNB1	[NCBI]	8.45608e-07
HGF	[NCBI]	8.39372e-07
VWF	[NCBI]	7.87732e-07
CCK	[NCBI]	7.57666e-07
CDKN1A	[NCBI]	6.884e-07

OMIM	Link	Information gain
FA	[NCBI]	0.00160985
FANCB	[NCBI]	0.000252938
hla modifier	[NCBI]	0.000177262
intrauterine growth retardation with increased mitomycin c sensitivity	[NCBI]	0.00014568
hla-d histocompatibility type	[NCBI]	0.000130726
seckel syndrome 1	[NCBI]	0.000115704
ERCC1	[NCBI]	9.79999e-05
ED1	[NCBI]	7.8399e-05
BLM	[NCBI]	6.83941e-05
SDS	[NCBI]	6.47015e-05
AFP	[NCBI]	4.23788e-05
AT	[NCBI]	3.39539e-05
SLE	[NCBI]	3.30498e-05
CEACAM5	[NCBI]	3.15392e-05
PEPC	[NCBI]	3.02022e-05
XRCC2	[NCBI]	2.81386e-05
TNF	[NCBI]	2.60679e-05
IL2	[NCBI]	2.2441e-05
INHBA	[NCBI]	2.1865e-05
lymphoma, non-hodgkin, familial	[NCBI]	1.81954e-05
DHFR	[NCBI]	1.41e-05
PGR	[NCBI]	9.00931e-06
CYP1A1	[NCBI]	7.9231e-06
EPO	[NCBI]	6.16073e-06
XDH	[NCBI]	6.15764e-06
TYMS	[NCBI]	4.85039e-06
HGF	[NCBI]	1.65742e-06
CCK	[NCBI]	6.55548e-07