Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Jaw Diseases [NCBI]

Gene


 Gene Link Information
Gain		 01
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


 OMIM Link Information
gain		 01
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



Database Center for Life Science