|
OMIM |
Link |
Information gain |
01 |
|
neuropathy, hereditary motor and sensory, okinawa type
|
[NCBI]
|
0.00257456
|
|
|
hypertrophic neuropathy of dejerine-sottas
|
[NCBI]
|
0.00202988
|
|
|
neuropathy, hereditary motor and sensory, with excessive myelin folding complex, autosomal recessive
|
[NCBI]
|
0.00194338
|
|
|
PMP22
|
[NCBI]
|
0.00169371
|
|
|
neuropathy, hereditary motor and sensory, with deafness, mental retardation, and absent sensory large myelinated fibers
|
[NCBI]
|
0.00164346
|
|
|
hereditary motor and sensory neuropathy, type iic
|
[NCBI]
|
0.00134416
|
|
|
HMN1
|
[NCBI]
|
0.00128649
|
|
|
MPZ
|
[NCBI]
|
0.00119314
|
|
|
polyneuropathy, lethal neonatal, axonal sensorimotor, autosomal recessive
|
[NCBI]
|
0.00096756
|
|
|
SPOAN
|
[NCBI]
|
0.00096756
|
|
|
DSMA2
|
[NCBI]
|
0.00096756
|
|
|
HNPP
|
[NCBI]
|
0.00095858
|
|
|
RDPA
|
[NCBI]
|
0.000749926
|
|
|
spastic diplegia, infantile type
|
[NCBI]
|
0.000749926
|
|
|
cowchock syndrome
|
[NCBI]
|
0.000667984
|
|
|
DSMA3
|
[NCBI]
|
0.000614885
|
|
|
neuropathy, hereditary motor and sensory, russe type
|
[NCBI]
|
0.000518153
|
|
|
neuropathy, congenital hypomyelinating
|
[NCBI]
|
0.000484779
|
|
|
MTND4
|
[NCBI]
|
0.000472004
|
|
|
CMT4D
|
[NCBI]
|
0.000440228
|
|
|
leber optic atrophy, susceptibility to
|
[NCBI]
|
0.00039449
|
|
|
leber optic atrophy
|
[NCBI]
|
0.000354144
|
|
|
CMT1B
|
[NCBI]
|
0.000353461
|
|
|
CMT1A
|
[NCBI]
|
0.000334132
|
|
|
hereditary motor and sensory neuropathy vi
|
[NCBI]
|
0.00027649
|
|
|
GJB1
|
[NCBI]
|
0.000222191
|
|
|
neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive
|
[NCBI]
|
0.000175595
|
|
|
HMN2A
|
[NCBI]
|
0.000139529
|
|
|
EGR2
|
[NCBI]
|
0.0001359
|
|
|
spastic paraplegia with neuropathy and poikiloderma
|
[NCBI]
|
0.00011017
|
|
|
HMN2B
|
[NCBI]
|
0.00011017
|
|
|
neuropathy, hereditary thermosensitive
|
[NCBI]
|
0.00011017
|
|
|
optic atrophy, hearing loss, and peripheral neuropathy, autosomal dominant
|
[NCBI]
|
0.00011017
|
|
|
charcot-marie-tooth disease, dominant intermediate d
|
[NCBI]
|
0.00011017
|
|
|
GAN1
|
[NCBI]
|
0.00010794
|
|
|
GAN
|
[NCBI]
|
0.000107409
|
|
|
CMTX1
|
[NCBI]
|
9.58991e-05
|
|
|
NDRG1
|
[NCBI]
|
9.56559e-05
|
|
|
SPG3A
|
[NCBI]
|
9.24613e-05
|
|
|
slowed nerve conduction velocity, autosomal dominant
|
[NCBI]
|
8.77159e-05
|
|
|
HSPB1
|
[NCBI]
|
8.30345e-05
|
|
|
charcot-marie-tooth disease, axonal, type 2f
|
[NCBI]
|
7.92517e-05
|
|
|
keratoderma, palmoplantar, with nail dystrophy and hereditary motor-sensory neuropathy
|
[NCBI]
|
7.92517e-05
|
|
|
gonadal dysgenesis, 46,xy, partial, with minifascicular neuropathy
|
[NCBI]
|
7.37614e-05
|
|
|
NDRG3
|
[NCBI]
|
7.26222e-05
|
|
|
SLA
|
[NCBI]
|
7.26222e-05
|
|
|
CCT5
|
[NCBI]
|
7.26222e-05
|
|
|
ARHGEF10
|
[NCBI]
|
7.26222e-05
|
|
|
TNRC6A
|
[NCBI]
|
7.26222e-05
|
|
|
bile acid synthesis defect, congenital, 4
|
[NCBI]
|
6.96835e-05
|
|
|
charcot-marie-tooth disease, axonal, type 2j
|
[NCBI]
|
6.64375e-05
|
|
|
SANDO
|
[NCBI]
|
6.37411e-05
|
|
|
NN
|
[NCBI]
|
6.37411e-05
|
|
|
ALS4
|
[NCBI]
|
6.37411e-05
|
|
|
CMT4B1
|
[NCBI]
|
6.14354e-05
|
|
|
CMT4B2
|
[NCBI]
|
5.94218e-05
|
|
|
NDRG2
|
[NCBI]
|
5.88481e-05
|
|
|
HAM
|
[NCBI]
|
5.7635e-05
|
|
|
TTR
|
[NCBI]
|
5.72481e-05
|
|
|
SPG17
|
[NCBI]
|
5.60292e-05
|
|
|
trifunctional protein deficiency
|
[NCBI]
|
5.45716e-05
|
|
|
ARF3
|
[NCBI]
|
5.36533e-05
|
|
|
TST
|
[NCBI]
|
5.36533e-05
|
|
|
NINJ1
|
[NCBI]
|
5.36533e-05
|
|
|
ACCPN
|
[NCBI]
|
5.32371e-05
|
|
|
HMN5
|
[NCBI]
|
5.2007e-05
|
|
|
DSMA1
|
[NCBI]
|
5.08662e-05
|
|
|
COX10
|
[NCBI]
|
4.7777e-05
|
|
|
HSPB8
|
[NCBI]
|
4.5782e-05
|
|
|
SBF2
|
[NCBI]
|
4.5782e-05
|
|
|
SPG2
|
[NCBI]
|
4.53595e-05
|
|
|
EAOH
|
[NCBI]
|
4.38862e-05
|
|
|
long-chain 3-hydroxyacyl-coa dehydrogenase deficiency
|
[NCBI]
|
4.38862e-05
|
|
|
AAA
|
[NCBI]
|
4.31993e-05
|
|
|
HNA
|
[NCBI]
|
4.31993e-05
|
|
|
PRPH
|
[NCBI]
|
4.27058e-05
|
|
|
IGHMBP2
|
[NCBI]
|
4.14666e-05
|
|
|
BSCL2
|
[NCBI]
|
4.03664e-05
|
|
|
CGL2
|
[NCBI]
|
4.0162e-05
|
|
|
PRX
|
[NCBI]
|
3.68976e-05
|
|
|
HADHA
|
[NCBI]
|
3.61936e-05
|
|
|
MAG
|
[NCBI]
|
3.48507e-05
|
|
|
ATXN8OS
|
[NCBI]
|
3.06535e-05
|
|
|
GCH1
|
[NCBI]
|
2.99161e-05
|
|
|
REN
|
[NCBI]
|
2.85926e-05
|
|
|
GSN
|
[NCBI]
|
2.82886e-05
|
|
|
POLG
|
[NCBI]
|
2.66442e-05
|
|
|
MTATP6
|
[NCBI]
|
2.63959e-05
|
|
|
AMACR
|
[NCBI]
|
2.44152e-05
|
|
|
NS1
|
[NCBI]
|
2.14689e-05
|
|
|
MB
|
[NCBI]
|
1.57715e-05
|
|
|
dystrophia myotonica 1
|
[NCBI]
|
9.71884e-06
|
|
|
MJD
|
[NCBI]
|
8.48476e-06
|
|
|
MBP
|
[NCBI]
|
3.25918e-06
|
|
|
GFAP
|
[NCBI]
|
8.43455e-07
|
|
|
TG
|
[NCBI]
|
5.38888e-07
|
|
|
AR
|
[NCBI]
|
1.98695e-07
|
|