Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Tooth Root	[NCBI]

Gene	Link	Information Gain
IBSP	[NCBI]	0.000121197
ACP5	[NCBI]	4.67899e-05
BMP7	[NCBI]	1.73988e-05
AMBN	[NCBI]	5.86066e-06
MMP20	[NCBI]	5.8236e-06
NPY	[NCBI]	5.79368e-06
CDC73	[NCBI]	5.56821e-06
BMP2	[NCBI]	5.32726e-06
DMP1	[NCBI]	5.05201e-06
PDGFB	[NCBI]	4.49941e-06
ENPP1	[NCBI]	4.35611e-06
DSPP	[NCBI]	4.33957e-06
PCNA	[NCBI]	3.96084e-06
IL1A	[NCBI]	3.86622e-06
EGF	[NCBI]	3.44232e-06
DBH	[NCBI]	3.35182e-06
MMP13	[NCBI]	3.22241e-06
FGF7	[NCBI]	3.12238e-06
IGF1	[NCBI]	3.09428e-06
LAMB3	[NCBI]	2.97909e-06
NOG	[NCBI]	2.77333e-06
CD68	[NCBI]	1.91638e-06
MPO	[NCBI]	1.42896e-06

OMIM	Link	Information gain
dentin dysplasia, type i	[NCBI]	0.00302164
dentin dysplasia with sclerotic bones	[NCBI]	0.0017631
mohr syndrome	[NCBI]	0.00103446
SPP1	[NCBI]	0.000384875
MCOPS2	[NCBI]	0.00032568
hypoplasia of teeth roots	[NCBI]	0.000240459
ackerman syndrome	[NCBI]	0.000240459
tooth size	[NCBI]	0.000201187
taurodontism	[NCBI]	0.000186368
ACP5	[NCBI]	0.000169725
dentinogenesis imperfecta, shields type iii	[NCBI]	0.000151553
immunoosseous dysplasia, schimke type	[NCBI]	0.000151553
dyschromatosis symmetrica hereditaria 1	[NCBI]	0.00014064
trichodentoosseous syndrome	[NCBI]	0.000136444
DGI1	[NCBI]	0.000136444
RTS	[NCBI]	0.00011282
CCD	[NCBI]	9.40001e-05
NFIC	[NCBI]	5.26449e-05
DSPP	[NCBI]	2.5606e-05
NPY	[NCBI]	1.47396e-05
FGF7	[NCBI]	1.14172e-05
PCNA	[NCBI]	1.06879e-05
SHH	[NCBI]	7.4895e-06
EGF	[NCBI]	3.02115e-06
MPO	[NCBI]	2.20245e-06