MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Cleidocranial Dysplasia
[NCBI]
Gene
Gene
Link
Information
Gain
01
RUNX2
[NCBI]
0.000449004
RUNX1
[NCBI]
3.6789e-05
SMAD3
[NCBI]
1.39632e-05
OSTF1
[NCBI]
1.269e-05
MSX2
[NCBI]
1.02603e-05
ALX4
[NCBI]
1.017e-05
VEGFB
[NCBI]
9.70974e-06
SMAD1
[NCBI]
8.37678e-06
BMP6
[NCBI]
8.09315e-06
EDA
[NCBI]
7.3441e-06
FGF4
[NCBI]
7.29434e-06
RUNX3
[NCBI]
7.19898e-06
SHOX
[NCBI]
6.99534e-06
IBSP
[NCBI]
6.20066e-06
CKAP4
[NCBI]
5.60791e-06
TP63
[NCBI]
4.88732e-06
BMP2
[NCBI]
4.45522e-06
LIF
[NCBI]
4.15596e-06
VEGFA
[NCBI]
2.07063e-06
OMIM
OMIM
Link
Information
gain
01
CCD
[NCBI]
0.00966752
cleidocranial dysplasia with micrognathia, absent thumbs, and distal aphalangia
[NCBI]
0.00423007
RUNX2
[NCBI]
0.00123849
acrodysostosis
[NCBI]
0.000705355
pycnodysostosis
[NCBI]
0.000125063
hypophosphatasia, adult type
[NCBI]
0.000123223
cleidocranial dysplasia, recessive form
[NCBI]
0.000113208
PFMCCD
[NCBI]
0.000113208
hypophosphatasia, infantile
[NCBI]
0.000101003
VEGFB
[NCBI]
6.6266e-05
ALX4
[NCBI]
6.00921e-05
CBFB
[NCBI]
6.00921e-05
MSX2
[NCBI]
5.53239e-05
PFM
[NCBI]
5.386e-05
crouzon syndrome
[NCBI]
4.91306e-05
TCOF1
[NCBI]
4.82111e-05
BMP2
[NCBI]
4.69163e-05
ALPL
[NCBI]
4.65199e-05
aspartylglucosaminuria
[NCBI]
4.47463e-05
andersen cardiodysrhythmic periodic paralysis
[NCBI]
4.31125e-05
RUNX1
[NCBI]
4.21875e-05
ODDD
[NCBI]
3.96565e-05
exostoses, multiple, type i
[NCBI]
3.79854e-05
WS1
[NCBI]
3.13879e-05
TCOF
[NCBI]
2.99447e-05
HGPS
[NCBI]
2.80216e-05
ACH
[NCBI]
2.1116e-05
BCNS
[NCBI]
1.62379e-05
MFS
[NCBI]
1.115e-05
Database Center for Life Science