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MeSH keywords -> Related genes, diseases (OMIM)


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01 Mandibular Diseases [NCBI]


Gene


Gene Link Information
Gain
01
BMP2 [NCBI] 6.00448e-05
ACP5 [NCBI] 2.94947e-05
BMP4 [NCBI] 1.56284e-05
TNFRSF11A [NCBI] 1.19829e-05
AATF [NCBI] 1.18594e-05
TNFSF11 [NCBI] 1.15072e-05
SH3BP2 [NCBI] 1.01452e-05
CALCR [NCBI] 1.00861e-05
CEACAM8 [NCBI] 9.97355e-06
KRT10 [NCBI] 8.56828e-06
GBA [NCBI] 7.66076e-06
FCGR2A [NCBI] 7.18504e-06
SHH [NCBI] 5.94455e-06
PTPN11 [NCBI] 5.89922e-06
IL1A [NCBI] 5.88931e-06
ALK [NCBI] 5.70695e-06
CDK4 [NCBI] 4.79816e-06
IL1B [NCBI] 4.52958e-06
TNFRSF11B [NCBI] 4.51445e-06
PTHLH [NCBI] 4.30478e-06
CD68 [NCBI] 3.53173e-06
VWF [NCBI] 2.81466e-06
MPO [NCBI] 2.71206e-06
PCNA [NCBI] 2.48961e-06
PTH [NCBI] 1.89953e-06
EGF [NCBI] 1.7732e-06
TNF [NCBI] 8.90583e-07




OMIM


OMIM Link Information
gain
01
torus palatinus and torus mandibularis [NCBI] 0.000938013
acroosteolysis with osteoporosis and changes in skull and mandible [NCBI] 0.000672411
OSCS [NCBI] 0.000672411
BCNS [NCBI] 0.000472332
klippel-trenaunay-weber syndrome [NCBI] 0.00040697
CRMO [NCBI] 0.000203903
GDD [NCBI] 0.000193555
MAS [NCBI] 0.000101791
OGD [NCBI] 8.20324e-05
noonan-like/multiple giant cell lesion syndrome [NCBI] 7.86125e-05
cerebrocostomandibular syndrome [NCBI] 7.33947e-05
HRPT2 [NCBI] 6.94617e-05
MADA [NCBI] 6.42893e-05
camurati-engelmann disease [NCBI] 6.19444e-05
CVS [NCBI] 5.80894e-05
AMC [NCBI] 4.84579e-05
FGFR1 [NCBI] 4.40056e-05
GBA [NCBI] 4.40056e-05
CD [NCBI] 4.00591e-05
SHH [NCBI] 3.07419e-05
RA [NCBI] 2.86034e-05
TS [NCBI] 1.73016e-05
MPO [NCBI] 1.25029e-05
PCNA [NCBI] 1.11567e-05
PTH [NCBI] 7.9829e-06
EGF [NCBI] 7.16328e-06
TNF [NCBI] 3.76594e-06
VEGF [NCBI] 3.04201e-06




Database Center for Life Science