Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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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