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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