Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Tooth Eruption	[NCBI]

Gene	Link	Information Gain
ACP5	[NCBI]	3.28222e-05
EGF	[NCBI]	3.18386e-05
BMP2	[NCBI]	5.65759e-06
CRCT1	[NCBI]	3.98887e-06
TNFRSF11B	[NCBI]	3.83924e-06
CALB1	[NCBI]	3.11733e-06
CSF1	[NCBI]	2.57967e-06
EDA	[NCBI]	2.52792e-06
PTH	[NCBI]	2.35968e-06
GHR	[NCBI]	2.02526e-06
IBSP	[NCBI]	1.82058e-06
TNFRSF11A	[NCBI]	1.63605e-06
PRKCB	[NCBI]	1.61029e-06
TNFSF11	[NCBI]	1.57303e-06
EGFR	[NCBI]	8.52934e-07
NGF	[NCBI]	7.90193e-07
TNF	[NCBI]	5.09415e-07

OMIM	Link	Information gain
molar i reinclusion	[NCBI]	0.00224616
gapo syndrome	[NCBI]	0.000942438
robinow syndrome, autosomal dominant	[NCBI]	0.000844761
CCD	[NCBI]	0.000602781
SRS	[NCBI]	0.000327956
TNFRSF11B	[NCBI]	0.000202669
hypoplasia of teeth roots	[NCBI]	0.000166738
dental noneruption	[NCBI]	0.000166738
ACP5	[NCBI]	0.000163655
EGF	[NCBI]	0.00015576
tooth size	[NCBI]	0.000138969
teeth present at birth	[NCBI]	0.000138969
IP	[NCBI]	0.000135967
steatocystoma multiplex with natal teeth	[NCBI]	0.000128491
PC2	[NCBI]	0.00011663
seckel syndrome 1	[NCBI]	9.18662e-05
EVC	[NCBI]	8.11712e-05
ED1	[NCBI]	6.75964e-05
PTHLH	[NCBI]	6.06571e-05
WHS	[NCBI]	5.6438e-05
TNFSF11	[NCBI]	4.3165e-05
CPI	[NCBI]	4.23284e-05
FOS	[NCBI]	2.67504e-05
VEGF	[NCBI]	1.40847e-05
GHR	[NCBI]	1.23648e-05
SHH	[NCBI]	5.60653e-06
PTH	[NCBI]	3.70779e-06
TNF	[NCBI]	8.97511e-07
EGFR	[NCBI]	2.20336e-07
NGFB	[NCBI]	1.24795e-09