MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Myelin P0 Protein
[NCBI]
Gene
Gene
Link
Information
Gain
01
MPZ
[NCBI]
0.000269301
PMP22
[NCBI]
0.00017393
GJB1
[NCBI]
7.73832e-05
MS
[NCBI]
5.5892e-05
MBP
[NCBI]
3.90126e-05
EGR2
[NCBI]
1.22942e-05
GDAP1
[NCBI]
7.09514e-06
MAG
[NCBI]
6.4257e-06
LITAF
[NCBI]
5.31959e-06
NEFL
[NCBI]
4.90529e-06
GFAP
[NCBI]
4.34922e-06
MAD2L1BP
[NCBI]
3.62003e-06
MTMR2
[NCBI]
3.35207e-06
KIF1B
[NCBI]
3.26272e-06
POU3F1
[NCBI]
3.19821e-06
MFN2
[NCBI]
2.96551e-06
MOG
[NCBI]
2.82118e-06
SOX10
[NCBI]
2.65772e-06
SIGLEC1
[NCBI]
2.60326e-06
NEFM
[NCBI]
2.27728e-06
RAB7A
[NCBI]
2.27299e-06
NEFH
[NCBI]
1.88201e-06
CDRT1
[NCBI]
1.72913e-06
PRB4
[NCBI]
1.72913e-06
MYRIP
[NCBI]
1.72913e-06
MPZL1
[NCBI]
1.69217e-06
SH3TC2
[NCBI]
1.69217e-06
PLLP
[NCBI]
1.67545e-06
SBF2
[NCBI]
1.63078e-06
CNTNAP1
[NCBI]
1.63078e-06
PRX
[NCBI]
1.60467e-06
GAN
[NCBI]
1.59252e-06
MAL
[NCBI]
1.58089e-06
UBE4B
[NCBI]
1.56975e-06
PRPH
[NCBI]
1.53887e-06
RAG1
[NCBI]
1.53804e-06
CNTNAP2
[NCBI]
1.47064e-06
QKI
[NCBI]
1.46322e-06
MYT1
[NCBI]
1.456e-06
DNM2
[NCBI]
1.3513e-06
HSPB8
[NCBI]
1.34185e-06
NDRG1
[NCBI]
1.33725e-06
FXR1
[NCBI]
1.32828e-06
NCOA1
[NCBI]
1.1536e-06
GNB2L1
[NCBI]
1.11339e-06
CNTN1
[NCBI]
1.08903e-06
KLRB1
[NCBI]
1.07508e-06
CTNNB1
[NCBI]
1.02301e-06
PVR
[NCBI]
9.76959e-07
AR
[NCBI]
9.29208e-07
APOE
[NCBI]
8.81358e-07
LMNA
[NCBI]
8.73868e-07
ERG
[NCBI]
7.9091e-07
HSPB1
[NCBI]
7.61223e-07
CLU
[NCBI]
7.59192e-07
TNF
[NCBI]
6.99911e-07
CAV1
[NCBI]
6.6726e-07
IFNGR1
[NCBI]
6.1648e-07
PRKCA
[NCBI]
6.07183e-07
PAX6
[NCBI]
5.92167e-07
TF
[NCBI]
5.80483e-07
NGF
[NCBI]
1.53725e-07
EGF
[NCBI]
5.60483e-08
OMIM
OMIM
Link
Information
gain
01
MPZ
[NCBI]
0.0027687
hypertrophic neuropathy of dejerine-sottas
[NCBI]
0.00260041
neuropathy, congenital hypomyelinating
[NCBI]
0.00110724
charcot-marie-tooth disease, axonal, type 2j
[NCBI]
0.00100401
CMT1A
[NCBI]
0.000835148
PMP22
[NCBI]
0.000760753
MAG
[NCBI]
0.000715124
charcot-marie-tooth disease, axonal, type 2i
[NCBI]
0.000499502
CMT1B
[NCBI]
0.00040576
MBP
[NCBI]
0.000359947
GJB1
[NCBI]
0.000299343
roussy-levy hereditary areflexic dystasia
[NCBI]
0.000165967
charcot-marie-tooth disease, dominant intermediate d
[NCBI]
0.000165967
adie pupil
[NCBI]
0.000134391
charcot-marie-tooth disease and deafness
[NCBI]
0.000114755
CMT4B1
[NCBI]
0.000109013
charcot-marie-tooth disease, axonal, type 2b1
[NCBI]
0.00010444
EGR2
[NCBI]
7.11379e-05
KIF1B
[NCBI]
2.53371e-05
POU3F1
[NCBI]
2.30112e-05
MYT1
[NCBI]
2.18849e-05
DNM2
[NCBI]
2.14006e-05
GDAP1
[NCBI]
2.0957e-05
EGF
[NCBI]
2.07573e-05
NTRK3
[NCBI]
2.01682e-05
NTF3
[NCBI]
1.94823e-05
NEFL
[NCBI]
1.8597e-05
DHH
[NCBI]
1.62361e-05
GFAP
[NCBI]
1.30943e-05
NRG1
[NCBI]
9.46155e-06
NGFB
[NCBI]
7.81759e-06
NGFR
[NCBI]
7.57721e-06
TNF
[NCBI]
6.8421e-06
FMR1
[NCBI]
6.35082e-06
TF
[NCBI]
7.72666e-07
APOE
[NCBI]
3.85697e-07
AR
[NCBI]
2.11033e-07
Database Center for Life Science