MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Camurati-Engelmann Syndrome
[NCBI]
Gene
Gene
Link
Information
Gain
01
TGFB1
[NCBI]
0.000113887
ANO5
[NCBI]
3.36453e-05
SLC6A5
[NCBI]
1.37725e-05
NAV2
[NCBI]
1.37725e-05
ANO1
[NCBI]
1.32388e-05
SLC17A6
[NCBI]
1.32388e-05
GAS2
[NCBI]
1.32388e-05
NELL1
[NCBI]
1.28325e-05
HTATIP2
[NCBI]
1.13518e-05
SOST
[NCBI]
1.10073e-05
FANCF
[NCBI]
1.0343e-05
SLC26A2
[NCBI]
9.68312e-06
TGFBR1
[NCBI]
6.52217e-06
ACP5
[NCBI]
5.71363e-06
TNFRSF11A
[NCBI]
5.57709e-06
TNFSF11
[NCBI]
5.34023e-06
SOD1
[NCBI]
4.68431e-06
OMIM
OMIM
Link
Information
gain
01
GHDD
[NCBI]
0.00549522
camurati-engelmann disease
[NCBI]
0.00280069
TGFB1
[NCBI]
0.000417481
GDD
[NCBI]
0.000309105
ribbing disease
[NCBI]
0.000231686
craniodiaphyseal dysplasia, dominant
[NCBI]
0.000131018
peripheral dysostosis
[NCBI]
0.000100073
hyperostosis corticalis generalisata, benign form of worth, with torus palatinus
[NCBI]
7.8364e-05
TMEM16E
[NCBI]
7.79e-05
exostoses, multiple, type i
[NCBI]
5.54043e-05
BGLAP
[NCBI]
3.92113e-05
MAS
[NCBI]
3.77222e-05
ACP5
[NCBI]
2.79341e-05
Database Center for Life Science