|
OMIM |
Link |
Information gain |
01 |
|
PMP22
|
[NCBI]
|
0.00562555
|
|
|
CMT1A
|
[NCBI]
|
0.00487007
|
|
|
neuropathy, hereditary motor and sensory, russe type
|
[NCBI]
|
0.00403463
|
|
|
CMT2B2
|
[NCBI]
|
0.00374021
|
|
|
MPZ
|
[NCBI]
|
0.00318986
|
|
|
GJB1
|
[NCBI]
|
0.00295621
|
|
|
CMT1B
|
[NCBI]
|
0.00284549
|
|
|
CMTX3
|
[NCBI]
|
0.00279521
|
|
|
charcot-marie-tooth disease, dominant intermediate a
|
[NCBI]
|
0.00244195
|
|
|
CMTX1
|
[NCBI]
|
0.00236901
|
|
|
hereditary motor and sensory neuropathy, type iic
|
[NCBI]
|
0.00214251
|
|
|
hereditary motor and sensory neuropathy v
|
[NCBI]
|
0.0020452
|
|
|
CMTX2
|
[NCBI]
|
0.00185702
|
|
|
hypertrophic neuropathy of dejerine-sottas
|
[NCBI]
|
0.00155429
|
|
|
CMT4A
|
[NCBI]
|
0.00114128
|
|
|
CMT2B
|
[NCBI]
|
0.000990068
|
|
|
MFN2
|
[NCBI]
|
0.000887179
|
|
|
EGR2
|
[NCBI]
|
0.000811554
|
|
|
GDAP1
|
[NCBI]
|
0.000811379
|
|
|
CMT4C
|
[NCBI]
|
0.00080244
|
|
|
CMT2A2
|
[NCBI]
|
0.000770636
|
|
|
CMT2A1
|
[NCBI]
|
0.000725198
|
|
|
CMT4B2
|
[NCBI]
|
0.000708979
|
|
|
CMT2G
|
[NCBI]
|
0.000707844
|
|
|
giant axonal neuropathy, autosomal dominant
|
[NCBI]
|
0.000707844
|
|
|
NEFL
|
[NCBI]
|
0.000669357
|
|
|
neuropathy, congenital hypomyelinating
|
[NCBI]
|
0.000664915
|
|
|
neuropathy, hereditary motor and sensory, with deafness, mental retardation, and absent sensory large myelinated fibers
|
[NCBI]
|
0.000626005
|
|
|
cowchock syndrome
|
[NCBI]
|
0.000626005
|
|
|
CMT4B1
|
[NCBI]
|
0.000615809
|
|
|
CMT2D
|
[NCBI]
|
0.000587434
|
|
|
MPD2
|
[NCBI]
|
0.00057301
|
|
|
spinal muscular atrophy, distal, congenital nonprogressive
|
[NCBI]
|
0.00057301
|
|
|
amyotrophy, neurogenic scapuloperoneal, new england type
|
[NCBI]
|
0.000533713
|
|
|
scheuermann disease
|
[NCBI]
|
0.000533713
|
|
|
PRX
|
[NCBI]
|
0.000521849
|
|
|
HMN7A
|
[NCBI]
|
0.000476586
|
|
|
HNPP
|
[NCBI]
|
0.000459848
|
|
|
charcot-marie-tooth disease, axonal, type 2j
|
[NCBI]
|
0.000430636
|
|
|
GARS
|
[NCBI]
|
0.00041977
|
|
|
MTMR2
|
[NCBI]
|
0.00041977
|
|
|
HMN5
|
[NCBI]
|
0.000414869
|
|
|
charcot-marie-tooth disease, dominant intermediate b
|
[NCBI]
|
0.000406617
|
|
|
CMT1C
|
[NCBI]
|
0.000379404
|
|
|
charcot-marie-tooth disease, recessive intermediate a
|
[NCBI]
|
0.000379404
|
|
|
charcot-marie-tooth disease, axonal, with vocal cord paresis, autosomal recessive
|
[NCBI]
|
0.000379404
|
|
|
CMT4H
|
[NCBI]
|
0.000379404
|
|
|
microcephalic osteodysplastic primordial dwarfism, type i
|
[NCBI]
|
0.000334286
|
|
|
LITAF
|
[NCBI]
|
0.000334136
|
|
|
charcot-marie-tooth disease and deafness
|
[NCBI]
|
0.000317587
|
|
|
RAB7
|
[NCBI]
|
0.000305773
|
|
|
charcot-marie-tooth disease, axonal, type 2i
|
[NCBI]
|
0.000284458
|
|
|
charcot-marie-tooth disease, axonal, type 2e
|
[NCBI]
|
0.000284458
|
|
|
charcot-marie-tooth disease, axonal, type 2f
|
[NCBI]
|
0.000284458
|
|
|
SBF2
|
[NCBI]
|
0.000275284
|
|
|
KIF1B
|
[NCBI]
|
0.000275284
|
|
|
HMN2A
|
[NCBI]
|
0.000270583
|
|
|
SMS
|
[NCBI]
|
0.000251148
|
|
|
NDRG1
|
[NCBI]
|
0.000233344
|
|
|
charcot-marie-tooth disease, axonal, type 2b1
|
[NCBI]
|
0.00021718
|
|
|
HSPB8
|
[NCBI]
|
0.000203729
|
|
|
slowed nerve conduction velocity, autosomal dominant
|
[NCBI]
|
0.000189576
|
|
|
charcot-marie-tooth disease, dominant intermediate c
|
[NCBI]
|
0.000189576
|
|
|
charcot-marie-tooth disease, axonal, type 2l
|
[NCBI]
|
0.000189576
|
|
|
CMT1D
|
[NCBI]
|
0.000189576
|
|
|
CMT2K
|
[NCBI]
|
0.000189576
|
|
|
CMT4D
|
[NCBI]
|
0.000185759
|
|
|
SH3TC2
|
[NCBI]
|
0.000158854
|
|
|
FGD4
|
[NCBI]
|
0.000158854
|
|
|
CVT
|
[NCBI]
|
0.000144724
|
|
|
roussy-levy hereditary areflexic dystasia
|
[NCBI]
|
0.000135166
|
|
|
DNM2
|
[NCBI]
|
0.000128694
|
|
|
TNF
|
[NCBI]
|
0.000123056
|
|
|
NEF3
|
[NCBI]
|
0.000120764
|
|
|
PMP2
|
[NCBI]
|
0.000120764
|
|
|
YARS
|
[NCBI]
|
0.000120764
|
|
|
CDRT1
|
[NCBI]
|
0.000120764
|
|
|
HSPB1
|
[NCBI]
|
0.000100913
|
|
|
charcot-marie-tooth disease, axonal, type 2h
|
[NCBI]
|
9.47564e-05
|
|
|
charcot-marie-tooth peroneal muscular atrophy, x-linked, with aplasia cutis congenita
|
[NCBI]
|
9.47564e-05
|
|
|
CMT4J
|
[NCBI]
|
9.47564e-05
|
|
|
charcot-marie-tooth disease with ptosis and parkinsonism
|
[NCBI]
|
9.47564e-05
|
|
|
charcot-marie-tooth disease, demyelinating, type 1f
|
[NCBI]
|
9.47564e-05
|
|
|
charcot-marie-tooth disease, guadalajara neuronal type
|
[NCBI]
|
9.47564e-05
|
|
|
HMN2B
|
[NCBI]
|
9.47564e-05
|
|
|
COX10
|
[NCBI]
|
8.73819e-05
|
|
|
GAN
|
[NCBI]
|
8.28914e-05
|
|
|
REN
|
[NCBI]
|
8.28806e-05
|
|
|
GAN1
|
[NCBI]
|
7.76744e-05
|
|
|
keratoderma, palmoplantar, with nail dystrophy and hereditary motor-sensory neuropathy
|
[NCBI]
|
6.38953e-05
|
|
|
LAPTM5
|
[NCBI]
|
6.03674e-05
|
|
|
kiaa0274
|
[NCBI]
|
6.03674e-05
|
|
|
ZSCAN20
|
[NCBI]
|
6.03674e-05
|
|
|
ARHGEF10
|
[NCBI]
|
6.03674e-05
|
|
|
ACTR1A
|
[NCBI]
|
6.03674e-05
|
|
|
adie pupil
|
[NCBI]
|
5.84339e-05
|
|
|
CMTX5
|
[NCBI]
|
5.84339e-05
|
|
|
hereditary motor and sensory neuropathy vi
|
[NCBI]
|
5.43848e-05
|
|
|
SPMM
|
[NCBI]
|
4.85e-05
|
|
|
RPL9
|
[NCBI]
|
4.66095e-05
|
|
|
NEURL
|
[NCBI]
|
4.66095e-05
|
|
|
SCN2B
|
[NCBI]
|
4.66095e-05
|
|
|
DRP2
|
[NCBI]
|
4.66095e-05
|
|
|
INA
|
[NCBI]
|
4.66095e-05
|
|
|
RNU3
|
[NCBI]
|
4.66095e-05
|
|
|
HOXD10
|
[NCBI]
|
4.1431e-05
|
|
|
EMP1
|
[NCBI]
|
4.1431e-05
|
|
|
GABBR2
|
[NCBI]
|
4.1431e-05
|
|
|
TDP1
|
[NCBI]
|
4.1431e-05
|
|
|
NRG2
|
[NCBI]
|
4.1431e-05
|
|
|
NINJ1
|
[NCBI]
|
4.1431e-05
|
|
|
SOX14
|
[NCBI]
|
4.1431e-05
|
|
|
LGMD1B
|
[NCBI]
|
3.81691e-05
|
|
|
EMP3
|
[NCBI]
|
3.80761e-05
|
|
|
RSN
|
[NCBI]
|
3.80761e-05
|
|
|
EMP2
|
[NCBI]
|
3.80761e-05
|
|
|
PXN
|
[NCBI]
|
3.55872e-05
|
|
|
FCGR2A
|
[NCBI]
|
3.55872e-05
|
|
|
SDC3
|
[NCBI]
|
3.55872e-05
|
|
|
GJC2
|
[NCBI]
|
3.36085e-05
|
|
|
MG
|
[NCBI]
|
3.28001e-05
|
|
|
danon disease
|
[NCBI]
|
3.12862e-05
|
|
|
EDMD2
|
[NCBI]
|
2.97968e-05
|
|
|
NEFH
|
[NCBI]
|
2.93419e-05
|
|
|
HSAN1
|
[NCBI]
|
2.91066e-05
|
|
|
EAOH
|
[NCBI]
|
2.91066e-05
|
|
|
BSCL2
|
[NCBI]
|
2.8258e-05
|
|
|
EA2
|
[NCBI]
|
2.78198e-05
|
|
|
PMD
|
[NCBI]
|
2.74431e-05
|
|
|
LMNA
|
[NCBI]
|
2.64614e-05
|
|
|
TSG101
|
[NCBI]
|
2.64031e-05
|
|
|
FHM1
|
[NCBI]
|
2.40736e-05
|
|
|
OPA1
|
[NCBI]
|
2.40736e-05
|
|
|
FPLD2
|
[NCBI]
|
2.31694e-05
|
|
|
FY
|
[NCBI]
|
1.95714e-05
|
|
|
CMD1A
|
[NCBI]
|
1.94037e-05
|
|
|
SOX10
|
[NCBI]
|
1.918e-05
|
|
|
HYPP
|
[NCBI]
|
1.90822e-05
|
|
|
SCA6
|
[NCBI]
|
1.84633e-05
|
|
|
sotos syndrome
|
[NCBI]
|
1.60172e-05
|
|
|
SCN4A
|
[NCBI]
|
1.47753e-05
|
|
|
MTATP6
|
[NCBI]
|
1.47753e-05
|
|
|
APCS
|
[NCBI]
|
1.45497e-05
|
|
|
dystrophia myotonica 1
|
[NCBI]
|
1.36541e-05
|
|
|
MAG
|
[NCBI]
|
1.3571e-05
|
|
|
PLP1
|
[NCBI]
|
1.20801e-05
|
|
|
SCA2
|
[NCBI]
|
1.14757e-05
|
|
|
SPTA1
|
[NCBI]
|
1.1455e-05
|
|
|
SCA1
|
[NCBI]
|
8.61824e-06
|
|
|
AGER
|
[NCBI]
|
4.98065e-06
|
|
|
GFAP
|
[NCBI]
|
4.77198e-06
|
|
|
MBP
|
[NCBI]
|
4.48854e-06
|
|
|
BCNS
|
[NCBI]
|
3.22107e-06
|
|
|
HD
|
[NCBI]
|
9.85461e-07
|
|
|
TTR
|
[NCBI]
|
4.7603e-07
|
|
|
NF1
|
[NCBI]
|
3.68215e-07
|
|
|
GDNF
|
[NCBI]
|
1.65836e-07
|
|
|
AT
|
[NCBI]
|
1.57839e-08
|
|