|
OMIM |
Link |
Information gain |
01 |
|
neuropathy, hereditary motor and sensory, russe type
|
[NCBI]
|
0.00277021
|
|
|
EGR2
|
[NCBI]
|
0.000678506
|
|
|
hypertrophic neuropathy of dejerine-sottas
|
[NCBI]
|
0.000408068
|
|
|
neuropathy, congenital hypomyelinating
|
[NCBI]
|
0.00029663
|
|
|
CMT1D
|
[NCBI]
|
0.000181535
|
|
|
charcot-marie-tooth disease, axonal, type 2i
|
[NCBI]
|
0.000169613
|
|
|
charcot-marie-tooth disease and deafness
|
[NCBI]
|
0.000161871
|
|
|
MPZ
|
[NCBI]
|
0.000130151
|
|
|
NAB1
|
[NCBI]
|
0.000117636
|
|
|
CMT1B
|
[NCBI]
|
0.000114862
|
|
|
CMT1A
|
[NCBI]
|
0.000100607
|
|
|
NAB2
|
[NCBI]
|
8.29237e-05
|
|
|
PMP22
|
[NCBI]
|
8.23823e-05
|
|
|
TNFSF6
|
[NCBI]
|
7.40049e-05
|
|
|
GJB1
|
[NCBI]
|
6.4746e-05
|
|
|
ZNF161
|
[NCBI]
|
4.65146e-05
|
|
|
SRF
|
[NCBI]
|
4.32305e-05
|
|
|
ABTB1
|
[NCBI]
|
3.6291e-05
|
|
|
KLF12
|
[NCBI]
|
3.44723e-05
|
|
|
CDH6
|
[NCBI]
|
3.31201e-05
|
|
|
KLF9
|
[NCBI]
|
3.31201e-05
|
|
|
EGR3
|
[NCBI]
|
3.1147e-05
|
|
|
POU3F1
|
[NCBI]
|
2.971e-05
|
|
|
MBP
|
[NCBI]
|
2.92046e-05
|
|
|
LITAF
|
[NCBI]
|
2.91147e-05
|
|
|
DNM2
|
[NCBI]
|
2.80926e-05
|
|
|
GDAP1
|
[NCBI]
|
2.76468e-05
|
|
|
ATF1
|
[NCBI]
|
2.6163e-05
|
|
|
TSC22D3
|
[NCBI]
|
2.50039e-05
|
|
|
PINK1
|
[NCBI]
|
2.42751e-05
|
|
|
DHH
|
[NCBI]
|
2.28851e-05
|
|
|
ALDH1A2
|
[NCBI]
|
2.28851e-05
|
|
|
EGR1
|
[NCBI]
|
2.1119e-05
|
|
|
ADCYAP1
|
[NCBI]
|
1.96446e-05
|
|
|
NGFR
|
[NCBI]
|
1.39178e-05
|
|
|
MAG
|
[NCBI]
|
8.48284e-06
|
|
|
VIP
|
[NCBI]
|
5.64069e-06
|
|
|
GFAP
|
[NCBI]
|
5.87196e-07
|
|