MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Vocal Cords
[NCBI]
Gene
Gene
Link
Information
Gain
01
HMN7A
[NCBI]
0.000466155
MPD2
[NCBI]
0.000466155
GER
[NCBI]
0.000102676
HGF
[NCBI]
2.92263e-05
EGFR
[NCBI]
8.58992e-06
EN1
[NCBI]
6.39446e-06
MYOT
[NCBI]
6.3061e-06
ASAH1
[NCBI]
5.89573e-06
HAS2
[NCBI]
5.51226e-06
PCNA
[NCBI]
5.40101e-06
KRT5
[NCBI]
5.31629e-06
TFF3
[NCBI]
5.26528e-06
TGM1
[NCBI]
4.85526e-06
KRT14
[NCBI]
4.84217e-06
MYOG
[NCBI]
4.83568e-06
MMP1
[NCBI]
4.42791e-06
VCAN
[NCBI]
4.37774e-06
TFF2
[NCBI]
4.18563e-06
NME1
[NCBI]
4.0191e-06
TFF1
[NCBI]
3.86929e-06
IL1B
[NCBI]
3.77186e-06
MMP9
[NCBI]
3.73713e-06
TOP2A
[NCBI]
3.71187e-06
ABCG2
[NCBI]
3.5853e-06
CD68
[NCBI]
2.62498e-06
MS
[NCBI]
2.50506e-06
CDKN1A
[NCBI]
1.65919e-06
NPY
[NCBI]
1.57797e-06
EGF
[NCBI]
8.29856e-07
OMIM
OMIM
Link
Information
gain
01
HMN7A
[NCBI]
0.00321518
MPD2
[NCBI]
0.00137599
hereditary motor and sensory neuropathy, type iic
[NCBI]
0.0012742
laryngeal abductor paralysis with cerebellar ataxia and motor neuropathy
[NCBI]
0.000246451
multiple pterygium syndrome, aslan type
[NCBI]
0.000207178
plasminogen deficiency, type i
[NCBI]
0.00016988
epidermolysis bullosa herpetiformis, dowling-meara type
[NCBI]
0.00016988
lipoid proteinosis of urbach and wiethe
[NCBI]
0.000142421
HGF
[NCBI]
0.000140777
MJD
[NCBI]
7.61832e-05
TTID
[NCBI]
4.66334e-05
PD
[NCBI]
4.64316e-05
KRT5
[NCBI]
3.76942e-05
KRT14
[NCBI]
3.76942e-05
EGFR
[NCBI]
3.49804e-05
PLG
[NCBI]
2.6549e-05
SDC2
[NCBI]
1.94108e-05
PCNA
[NCBI]
1.8727e-05
MUC1
[NCBI]
1.64973e-05
RA
[NCBI]
6.37899e-06
NPY
[NCBI]
2.50024e-06
SLE
[NCBI]
8.37634e-07
EGF
[NCBI]
3.47876e-08
Database Center for Life Science