|
OMIM |
Link |
Information gain |
01 |
|
neuropathy, hereditary motor and sensory, with deafness, mental retardation, and absent sensory large myelinated fibers
|
[NCBI]
|
0.00306272
|
|
|
polyneuropathy, lethal neonatal, axonal sensorimotor, autosomal recessive
|
[NCBI]
|
0.0015153
|
|
|
indifference to pain, congenital, autosomal dominant
|
[NCBI]
|
0.0015153
|
|
|
neuropathy, hereditary motor and sensory, with excessive myelin folding complex, autosomal recessive
|
[NCBI]
|
0.00120455
|
|
|
neuropathy, hereditary motor and sensory, russe type
|
[NCBI]
|
0.000910064
|
|
|
kohlschutter-tonz syndrome
|
[NCBI]
|
0.000910064
|
|
|
AMCN
|
[NCBI]
|
0.000812961
|
|
|
HSAN5
|
[NCBI]
|
0.000529354
|
|
|
MBP
|
[NCBI]
|
0.000527875
|
|
|
MAG
|
[NCBI]
|
0.000428838
|
|
|
MPZ
|
[NCBI]
|
0.000259495
|
|
|
AD
|
[NCBI]
|
0.000240813
|
|
|
hypertrophic neuropathy of dejerine-sottas
|
[NCBI]
|
0.000229501
|
|
|
SACS
|
[NCBI]
|
0.000217939
|
|
|
CMT4D
|
[NCBI]
|
0.000217939
|
|
|
DSMA1
|
[NCBI]
|
0.000205353
|
|
|
neuropathy, congenital hypomyelinating
|
[NCBI]
|
0.000186463
|
|
|
insensitivity to pain with hyperplastic myelinopathy
|
[NCBI]
|
0.00017617
|
|
|
neuropathy, hereditary sensory, x-linked
|
[NCBI]
|
0.00017617
|
|
|
VWM
|
[NCBI]
|
0.000169415
|
|
|
GAN1
|
[NCBI]
|
0.000156446
|
|
|
PMD
|
[NCBI]
|
0.000154582
|
|
|
HSAN3
|
[NCBI]
|
0.000147929
|
|
|
CMTX1
|
[NCBI]
|
0.00014413
|
|
|
slowed nerve conduction velocity, autosomal dominant
|
[NCBI]
|
0.000136949
|
|
|
charcot-marie-tooth disease, axonal, type 2e
|
[NCBI]
|
0.000136949
|
|
|
PMP22
|
[NCBI]
|
0.000136664
|
|
|
CMT1B
|
[NCBI]
|
0.00012976
|
|
|
ARTS
|
[NCBI]
|
0.000122181
|
|
|
gonadal dysgenesis, 46,xy, partial, with minifascicular neuropathy
|
[NCBI]
|
0.000122181
|
|
|
muscular dystrophy, congenital, with severe central nervous system atrophy and absence of large myelinated fibers
|
[NCBI]
|
0.000122181
|
|
|
SLE
|
[NCBI]
|
0.000118378
|
|
|
ALD
|
[NCBI]
|
0.000116888
|
|
|
roussy-levy hereditary areflexic dystasia
|
[NCBI]
|
0.00011261
|
|
|
charcot-marie-tooth disease, axonal, with vocal cord paresis, autosomal recessive
|
[NCBI]
|
0.00011261
|
|
|
GFAP
|
[NCBI]
|
0.000112376
|
|
|
SANDO
|
[NCBI]
|
0.000105507
|
|
|
l-2-hydroxyglutaric aciduria
|
[NCBI]
|
0.000105507
|
|
|
NN
|
[NCBI]
|
9.98584e-05
|
|
|
3-@methylglutaconic aciduria, type i
|
[NCBI]
|
9.98584e-05
|
|
|
APBD
|
[NCBI]
|
9.51704e-05
|
|
|
CMT4B2
|
[NCBI]
|
9.51704e-05
|
|
|
de sanctis-cacchione syndrome
|
[NCBI]
|
9.51704e-05
|
|
|
PLSJ
|
[NCBI]
|
9.51704e-05
|
|
|
lipomatosis, familial benign cervical
|
[NCBI]
|
9.11653e-05
|
|
|
SPG17
|
[NCBI]
|
9.11653e-05
|
|
|
CMT4B1
|
[NCBI]
|
9.11653e-05
|
|
|
CMT4C
|
[NCBI]
|
9.11653e-05
|
|
|
PRX
|
[NCBI]
|
9.05004e-05
|
|
|
congenital cataracts, facial dysmorphism, and neuropathy
|
[NCBI]
|
8.17907e-05
|
|
|
metachromatic leukodystrophy due to saposin b deficiency
|
[NCBI]
|
7.92677e-05
|
|
|
HHS
|
[NCBI]
|
7.92677e-05
|
|
|
HMN5
|
[NCBI]
|
7.92677e-05
|
|
|
HSAN2
|
[NCBI]
|
7.92677e-05
|
|
|
CMT4A
|
[NCBI]
|
7.92677e-05
|
|
|
FXTAS
|
[NCBI]
|
7.92677e-05
|
|
|
propionic acidemia
|
[NCBI]
|
7.69602e-05
|
|
|
AGS1
|
[NCBI]
|
7.69602e-05
|
|
|
krabbe disease
|
[NCBI]
|
7.68337e-05
|
|
|
NGFB
|
[NCBI]
|
7.4736e-05
|
|
|
NTRK1
|
[NCBI]
|
6.9728e-05
|
|
|
HSAN1
|
[NCBI]
|
6.9316e-05
|
|
|
SPG3A
|
[NCBI]
|
6.77047e-05
|
|
|
glutaric acidemia i
|
[NCBI]
|
6.77047e-05
|
|
|
SACS
|
[NCBI]
|
6.68089e-05
|
|
|
TGD
|
[NCBI]
|
6.47505e-05
|
|
|
HNA
|
[NCBI]
|
6.47505e-05
|
|
|
NEFH
|
[NCBI]
|
6.16684e-05
|
|
|
CJD
|
[NCBI]
|
6.13225e-05
|
|
|
sialuria, finnish type
|
[NCBI]
|
6.08642e-05
|
|
|
ODDD
|
[NCBI]
|
5.96882e-05
|
|
|
BDNF
|
[NCBI]
|
5.89655e-05
|
|
|
MJD
|
[NCBI]
|
5.86617e-05
|
|
|
NEFL
|
[NCBI]
|
5.79016e-05
|
|
|
NTF3
|
[NCBI]
|
5.79016e-05
|
|
|
TRPV1
|
[NCBI]
|
5.59286e-05
|
|
|
CADASIL
|
[NCBI]
|
5.45035e-05
|
|
|
cerebrotendinous xanthomatosis
|
[NCBI]
|
5.45035e-05
|
|
|
EGR2
|
[NCBI]
|
5.40611e-05
|
|
|
XPA
|
[NCBI]
|
5.35826e-05
|
|
|
NEM3
|
[NCBI]
|
5.35826e-05
|
|
|
DHH
|
[NCBI]
|
4.91415e-05
|
|
|
SMA1
|
[NCBI]
|
4.39691e-05
|
|
|
FCMD
|
[NCBI]
|
4.33664e-05
|
|
|
NGFR
|
[NCBI]
|
4.25003e-05
|
|
|
TNF
|
[NCBI]
|
4.23101e-05
|
|
|
GDNF
|
[NCBI]
|
4.21169e-05
|
|
|
amyloidosis vi
|
[NCBI]
|
4.06376e-05
|
|
|
LRRN6A
|
[NCBI]
|
3.95877e-05
|
|
|
AT
|
[NCBI]
|
3.94886e-05
|
|
|
SLS
|
[NCBI]
|
3.8545e-05
|
|
|
VEGF
|
[NCBI]
|
3.73633e-05
|
|
|
AQP4
|
[NCBI]
|
3.59737e-05
|
|
|
CANX
|
[NCBI]
|
3.58268e-05
|
|
|
EIF2B1
|
[NCBI]
|
3.58268e-05
|
|
|
CMT1A
|
[NCBI]
|
3.53929e-05
|
|
|
ADAM22
|
[NCBI]
|
3.3387e-05
|
|
|
EIF2B3
|
[NCBI]
|
3.3387e-05
|
|
|
CNTNAP2
|
[NCBI]
|
3.3387e-05
|
|
|
AUH
|
[NCBI]
|
3.3387e-05
|
|
|
FRDA
|
[NCBI]
|
3.30088e-05
|
|
|
JAM3
|
[NCBI]
|
3.15747e-05
|
|
|
EIF2B4
|
[NCBI]
|
3.15747e-05
|
|
|
FGF14
|
[NCBI]
|
2.89335e-05
|
|
|
HTR1B
|
[NCBI]
|
2.89335e-05
|
|
|
lady bird late, drosophila, homolog of, 1
|
[NCBI]
|
2.89335e-05
|
|
|
GAN
|
[NCBI]
|
2.89335e-05
|
|
|
GJB1
|
[NCBI]
|
2.82169e-05
|
|
|
IGHMBP2
|
[NCBI]
|
2.79085e-05
|
|
|
TBCE
|
[NCBI]
|
2.79085e-05
|
|
|
MYT1
|
[NCBI]
|
2.79085e-05
|
|
|
EGF
|
[NCBI]
|
2.73628e-05
|
|
|
leber optic atrophy
|
[NCBI]
|
2.63126e-05
|
|
|
farber lipogranulomatosis
|
[NCBI]
|
2.55048e-05
|
|
|
NDRG1
|
[NCBI]
|
2.55048e-05
|
|
|
EIF2B5
|
[NCBI]
|
2.48566e-05
|
|
|
CNTF
|
[NCBI]
|
2.46506e-05
|
|
|
PRPS1
|
[NCBI]
|
2.42631e-05
|
|
|
FGF2
|
[NCBI]
|
2.39359e-05
|
|
|
ZS
|
[NCBI]
|
2.28513e-05
|
|
|
GCDH
|
[NCBI]
|
2.18759e-05
|
|
|
SMAX1
|
[NCBI]
|
2.13382e-05
|
|
|
ACHE
|
[NCBI]
|
2.09287e-05
|
|
|
ASPA
|
[NCBI]
|
1.89534e-05
|
|
|
RTN4R
|
[NCBI]
|
1.84441e-05
|
|
|
POLG
|
[NCBI]
|
1.82031e-05
|
|
|
SLC17A7
|
[NCBI]
|
1.77454e-05
|
|
|
AKR1B1
|
[NCBI]
|
1.75057e-05
|
|
|
ARSA
|
[NCBI]
|
1.71123e-05
|
|
|
MTND1
|
[NCBI]
|
1.67212e-05
|
|
|
TTR
|
[NCBI]
|
1.21846e-05
|
|
|
FMF
|
[NCBI]
|
9.53682e-06
|
|
|
PLG
|
[NCBI]
|
9.52551e-06
|
|
|
VIP
|
[NCBI]
|
7.528e-06
|
|
|
FMR1
|
[NCBI]
|
6.89573e-06
|
|
|
CCK
|
[NCBI]
|
6.89304e-06
|
|
|
lymphoma, non-hodgkin, familial
|
[NCBI]
|
6.21746e-06
|
|
|
SLC18A3
|
[NCBI]
|
5.77844e-06
|
|
|
TS
|
[NCBI]
|
4.02366e-06
|
|
|
HDC
|
[NCBI]
|
3.70955e-06
|
|
|
HGF
|
[NCBI]
|
3.42754e-06
|
|
|
SHH
|
[NCBI]
|
3.35977e-06
|
|
|
panencephalitis, subacute sclerosing
|
[NCBI]
|
1.73364e-06
|
|
|
GAL
|
[NCBI]
|
1.73133e-06
|
|
|
NPY
|
[NCBI]
|
2.60506e-07
|
|
|
EPO
|
[NCBI]
|
2.26231e-07
|
|
|
POMC
|
[NCBI]
|
2.00883e-07
|
|
|
APOE
|
[NCBI]
|
1.72066e-07
|
|
|
PTK2
|
[NCBI]
|
1.54113e-07
|
|
|
TH
|
[NCBI]
|
7.03468e-10
|
|