MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Paresis
[NCBI]
Gene
Gene
Link
Information
Gain
01
MS
[NCBI]
0.00022669
HFM
[NCBI]
0.000141293
WG
[NCBI]
0.000133008
PMP22
[NCBI]
3.28295e-05
IGAN
[NCBI]
3.02222e-05
CACNA1A
[NCBI]
1.57259e-05
ATP13A2
[NCBI]
1.26217e-05
ALG3
[NCBI]
1.24066e-05
ARHGDIB
[NCBI]
1.22155e-05
MYH1
[NCBI]
1.14891e-05
ATP6
[NCBI]
1.09805e-05
RTN4R
[NCBI]
1.07349e-05
AMPD1
[NCBI]
9.8133e-06
CTSA
[NCBI]
9.0102e-06
NOTCH4
[NCBI]
8.85067e-06
ATP1A2
[NCBI]
8.59201e-06
KRIT1
[NCBI]
8.46585e-06
PLP1
[NCBI]
8.32955e-06
MPZ
[NCBI]
7.94572e-06
CD40LG
[NCBI]
7.54772e-06
SPN
[NCBI]
7.3366e-06
CYP3A4
[NCBI]
5.70813e-06
ADAMTS13
[NCBI]
5.39991e-06
BMP2
[NCBI]
5.24815e-06
BDNF
[NCBI]
3.97102e-06
ACHE
[NCBI]
3.85788e-06
MBP
[NCBI]
3.48152e-06
PTH
[NCBI]
2.05926e-06
PTGS2
[NCBI]
2.05586e-06
OMIM
OMIM
Link
Information
gain
01
polymicrogyria, unilateral
[NCBI]
0.00266538
HFM
[NCBI]
0.000449081
brain small vessel disease with hemorrhage
[NCBI]
0.000114976
IP
[NCBI]
0.000106987
adie pupil
[NCBI]
0.000100992
LBSL
[NCBI]
0.000100992
CDG1D
[NCBI]
9.68989e-05
KRS
[NCBI]
9.68989e-05
charcot-marie-tooth disease, axonal, type 2j
[NCBI]
9.36381e-05
SPMM
[NCBI]
9.09269e-05
PLSJ
[NCBI]
8.3156e-05
sturge-weber syndrome
[NCBI]
8.3156e-05
STXBP1
[NCBI]
7.06867e-05
ALG3
[NCBI]
6.81758e-05
GRIA3
[NCBI]
6.30871e-05
CADASIL
[NCBI]
6.26034e-05
meningioma, familial
[NCBI]
6.0217e-05
AMPD1
[NCBI]
5.58717e-05
NF2
[NCBI]
5.41503e-05
HGPS
[NCBI]
5.13836e-05
MTATP6
[NCBI]
4.65908e-05
CSF3
[NCBI]
4.4764e-05
CACNA1A
[NCBI]
4.45577e-05
CJD
[NCBI]
4.21138e-05
MPZ
[NCBI]
3.86117e-05
PMP22
[NCBI]
3.23347e-05
ALD
[NCBI]
2.45041e-05
lymphoma, non-hodgkin, familial
[NCBI]
1.56856e-05
BDNF
[NCBI]
1.40694e-05
ACHE
[NCBI]
1.2993e-05
MBP
[NCBI]
1.11911e-05
AVP
[NCBI]
1.03266e-05
SLE
[NCBI]
8.21474e-06
PTH
[NCBI]
4.23734e-06
Database Center for Life Science