Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Jaw Diseases	[NCBI]

Gene	Link	Information Gain
FOP	[NCBI]	0.000271232
SH3BP2	[NCBI]	3.96004e-05
CD68	[NCBI]	1.93714e-05
PCNA	[NCBI]	1.60501e-05
TNFRSF11A	[NCBI]	1.40094e-05
TNFSF11	[NCBI]	1.35311e-05
FGF13	[NCBI]	1.21881e-05
ADAM8	[NCBI]	1.1708e-05
CYP2C8	[NCBI]	9.82269e-06
ADAM12	[NCBI]	9.79502e-06
IL17A	[NCBI]	9.66303e-06
SHH	[NCBI]	6.93363e-06
CCND1	[NCBI]	6.40091e-06
TNFRSF11B	[NCBI]	5.49173e-06
HIF1A	[NCBI]	4.24889e-06
EGFR	[NCBI]	2.77328e-06

OMIM	Link	Information gain
acrodysostosis	[NCBI]	0.00109818
BCNS	[NCBI]	0.000378864
temporal arteritis	[NCBI]	0.000348278
fibrosis of extraocular muscles, congenital, with synergistic divergence	[NCBI]	0.000100673
chands	[NCBI]	0.000100673
gigantiform cementoma, familial	[NCBI]	0.000100673
GDD	[NCBI]	8.279e-05
noonan-like/multiple giant cell lesion syndrome	[NCBI]	7.73439e-05
GINGF	[NCBI]	7.45252e-05
PCNA	[NCBI]	7.27516e-05
aceruloplasminemia	[NCBI]	7.10508e-05
crouzon syndrome	[NCBI]	6.73472e-05
PDP	[NCBI]	6.65411e-05
TCOF1	[NCBI]	5.91221e-05
ODDD	[NCBI]	5.77097e-05
hypophosphatasia, infantile	[NCBI]	5.72641e-05
WS1	[NCBI]	4.91858e-05
TCOF	[NCBI]	4.76813e-05
AMC	[NCBI]	4.72104e-05
HGPS	[NCBI]	4.56663e-05
FOP	[NCBI]	4.5252e-05
SMAX1	[NCBI]	3.53633e-05
APC	[NCBI]	3.0385e-05
EGFR	[NCBI]	1.02837e-05
KLK3	[NCBI]	8.6391e-06
VEGF	[NCBI]	3.92706e-06