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MeSH keywords -> Related genes, diseases (OMIM)


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01 Ear Diseases [NCBI]

Gene


 Gene Link Information
Gain		 01
GER [NCBI] 0.000158688
EGF [NCBI] 2.35551e-05
GNB1L [NCBI] 1.32214e-05
SEPT5 [NCBI] 1.16779e-05
S100A1 [NCBI] 1.13333e-05
CHD7 [NCBI] 1.06548e-05
KCNQ4 [NCBI] 1.01699e-05
CD3E [NCBI] 9.55548e-06
TBX1 [NCBI] 9.44828e-06
CTSA [NCBI] 9.07614e-06
CTNNB1 [NCBI] 8.89619e-06
VWF [NCBI] 8.42707e-06
MPO [NCBI] 8.21157e-06
MMP7 [NCBI] 7.62536e-06
MMP3 [NCBI] 6.93079e-06
FGF7 [NCBI] 6.83835e-06
TLR9 [NCBI] 6.82343e-06
MMP2 [NCBI] 5.7031e-06
GJB2 [NCBI] 5.06372e-06
GSTP1 [NCBI] 4.49183e-06
VIP [NCBI] 4.41829e-06
TLR4 [NCBI] 4.17761e-06
NOS2 [NCBI] 3.5698e-06
HGF [NCBI] 3.50628e-06
TGFB1 [NCBI] 3.14592e-06
TNF [NCBI] 1.07241e-06



OMIM


 OMIM Link Information
gain		 01
atresia of external auditory canal and conduction deafness [NCBI] 0.00107364
actinic prurigo [NCBI] 0.000840405
palatopharyngeal incompetence [NCBI] 0.000565777
ossified ear cartilages with mental deficiency, muscle wasting, and bony changes [NCBI] 0.000112852
hairy ears, y-linked [NCBI] 0.000107346
phace association [NCBI] 9.49564e-05
EGF [NCBI] 8.72256e-05
plasminogen deficiency, type i [NCBI] 8.54328e-05
ED2 [NCBI] 8.12332e-05
BOR1 [NCBI] 7.1734e-05
EVA [NCBI] 6.98047e-05
MATN1 [NCBI] 6.74106e-05
velocardiofacial syndrome [NCBI] 5.89884e-05
TBX1 [NCBI] 5.44865e-05
DGS [NCBI] 4.36725e-05
CPI [NCBI] 4.19437e-05
PAX3 [NCBI] 4.16085e-05
SLOS [NCBI] 4.06026e-05
IDUA [NCBI] 4.02379e-05
BWS [NCBI] 3.50526e-05
TLR4 [NCBI] 2.42676e-05
VIP [NCBI] 1.50331e-05
HGF [NCBI] 1.08315e-05
MPO [NCBI] 7.59094e-06
SLE [NCBI] 2.10988e-06
TNF [NCBI] 7.96201e-07
VEGF [NCBI] 4.33511e-07
CF [NCBI] 4.62737e-08



Database Center for Life Science