|
OMIM |
Link |
Information gain |
01 |
|
MBP
|
[NCBI]
|
0.00396582
|
|
|
MAG
|
[NCBI]
|
0.00170892
|
|
|
ALD
|
[NCBI]
|
0.00169954
|
|
|
spinocerebellar ataxia with rigidity and peripheral neuropathy
|
[NCBI]
|
0.000832846
|
|
|
pallidopyramidal syndrome
|
[NCBI]
|
0.000832846
|
|
|
opticocochleodentate degeneration
|
[NCBI]
|
0.000832846
|
|
|
AXPC1
|
[NCBI]
|
0.000697531
|
|
|
neuropathy, hereditary motor and sensory, okinawa type
|
[NCBI]
|
0.000697531
|
|
|
hereditary motor and sensory neuropathy v
|
[NCBI]
|
0.000600386
|
|
|
neuropathy, hereditary motor and sensory, russe type
|
[NCBI]
|
0.000600386
|
|
|
pelizaeus-merzbacher-like disease, autosomal recessive, 2
|
[NCBI]
|
0.000600386
|
|
|
SPG5A
|
[NCBI]
|
0.000558521
|
|
|
hypertrophic neuropathy of dejerine-sottas
|
[NCBI]
|
0.000517805
|
|
|
neuropathy, congenital hypomyelinating
|
[NCBI]
|
0.000509364
|
|
|
progeroid syndrome, neonatal
|
[NCBI]
|
0.000498592
|
|
|
AMCN
|
[NCBI]
|
0.000486675
|
|
|
PMD
|
[NCBI]
|
0.000484104
|
|
|
PMP22
|
[NCBI]
|
0.000419207
|
|
|
VWM
|
[NCBI]
|
0.000369094
|
|
|
MPZ
|
[NCBI]
|
0.000343601
|
|
|
hemophagocytic lymphohistiocytosis, familial, 1
|
[NCBI]
|
0.000308354
|
|
|
krabbe disease
|
[NCBI]
|
0.000264313
|
|
|
CMT1B
|
[NCBI]
|
0.000223705
|
|
|
EIF2B5
|
[NCBI]
|
0.000219444
|
|
|
RA
|
[NCBI]
|
0.000199707
|
|
|
GFAP
|
[NCBI]
|
0.000187445
|
|
|
PCWH
|
[NCBI]
|
0.000153486
|
|
|
charcot-marie-tooth disease, recessive intermediate a
|
[NCBI]
|
0.000153486
|
|
|
CMT4H
|
[NCBI]
|
0.000153486
|
|
|
canavan disease
|
[NCBI]
|
0.000149742
|
|
|
EGR2
|
[NCBI]
|
0.000147353
|
|
|
ABCD1
|
[NCBI]
|
0.000131421
|
|
|
VEGF
|
[NCBI]
|
0.000131323
|
|
|
QKI
|
[NCBI]
|
0.000122056
|
|
|
GJB1
|
[NCBI]
|
0.00011804
|
|
|
CMT4A
|
[NCBI]
|
0.00011107
|
|
|
HNPP
|
[NCBI]
|
0.000110768
|
|
|
GDAP1
|
[NCBI]
|
0.000108772
|
|
|
methionine adenosyltransferase deficiency
|
[NCBI]
|
0.000108277
|
|
|
SLE
|
[NCBI]
|
0.000106931
|
|
|
PLP1
|
[NCBI]
|
0.000103559
|
|
|
CMT1A
|
[NCBI]
|
9.99571e-05
|
|
|
megalencephaly with dysmyelination
|
[NCBI]
|
9.9139e-05
|
|
|
HSAN2
|
[NCBI]
|
9.71436e-05
|
|
|
FGD4
|
[NCBI]
|
9.45368e-05
|
|
|
PLOSL
|
[NCBI]
|
9.36049e-05
|
|
|
SPG2
|
[NCBI]
|
9.1976e-05
|
|
|
GJC2
|
[NCBI]
|
8.41767e-05
|
|
|
hypomyelination and congenital cataract
|
[NCBI]
|
7.67021e-05
|
|
|
deafness, nerve type, with mesenteric diverticula of small bowel and progressive sensory neuropathy
|
[NCBI]
|
7.67021e-05
|
|
|
spinal muscular atrophy, scapuloperoneal
|
[NCBI]
|
7.67021e-05
|
|
|
CMT1D
|
[NCBI]
|
7.67021e-05
|
|
|
CMTX1
|
[NCBI]
|
7.4357e-05
|
|
|
CADASIL
|
[NCBI]
|
7.26261e-05
|
|
|
MAT1A
|
[NCBI]
|
6.85227e-05
|
|
|
ARTS
|
[NCBI]
|
6.82557e-05
|
|
|
PRX
|
[NCBI]
|
6.52364e-05
|
|
|
pelizaeus-merzbacher-like disease, autosomal recessive, 1
|
[NCBI]
|
6.27831e-05
|
|
|
CMT1C
|
[NCBI]
|
6.27831e-05
|
|
|
neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive
|
[NCBI]
|
6.27831e-05
|
|
|
charcot-marie-tooth disease, axonal, with vocal cord paresis, autosomal recessive
|
[NCBI]
|
6.27831e-05
|
|
|
CSA
|
[NCBI]
|
6.2124e-05
|
|
|
MAT2A
|
[NCBI]
|
6.10119e-05
|
|
|
charcot-marie-tooth disease and deafness
|
[NCBI]
|
5.54945e-05
|
|
|
gliosis, familial progressive subcortical
|
[NCBI]
|
5.54945e-05
|
|
|
SOX10
|
[NCBI]
|
5.32685e-05
|
|
|
cataract, microcephaly, failure to thrive, kyphoscoliosis syndrome
|
[NCBI]
|
5.28159e-05
|
|
|
hyperpipecolatemia
|
[NCBI]
|
5.05279e-05
|
|
|
SMA1
|
[NCBI]
|
4.87855e-05
|
|
|
ALS1
|
[NCBI]
|
4.87855e-05
|
|
|
CMT4B2
|
[NCBI]
|
4.8532e-05
|
|
|
spinal muscular atrophy, proximal, adult, autosomal dominant
|
[NCBI]
|
4.8532e-05
|
|
|
XPB
|
[NCBI]
|
4.8532e-05
|
|
|
SCARB2
|
[NCBI]
|
4.72526e-05
|
|
|
DRP2
|
[NCBI]
|
4.72526e-05
|
|
|
OLIG1
|
[NCBI]
|
4.72526e-05
|
|
|
CMT4C
|
[NCBI]
|
4.67628e-05
|
|
|
CMT4D
|
[NCBI]
|
4.67628e-05
|
|
|
BPP
|
[NCBI]
|
4.67628e-05
|
|
|
GS2
|
[NCBI]
|
4.37348e-05
|
|
|
EGFR
|
[NCBI]
|
4.33734e-05
|
|
|
ACCPN
|
[NCBI]
|
4.24181e-05
|
|
|
leprosy, susceptibility to
|
[NCBI]
|
4.12056e-05
|
|
|
DSMA1
|
[NCBI]
|
4.00825e-05
|
|
|
FGF2
|
[NCBI]
|
3.88557e-05
|
|
|
ZS
|
[NCBI]
|
3.76662e-05
|
|
|
MS
|
[NCBI]
|
3.74305e-05
|
|
|
INAD1
|
[NCBI]
|
3.71403e-05
|
|
|
SHH
|
[NCBI]
|
3.62896e-05
|
|
|
alexander disease
|
[NCBI]
|
3.54571e-05
|
|
|
SBF2
|
[NCBI]
|
3.42458e-05
|
|
|
RTN4R
|
[NCBI]
|
3.42458e-05
|
|
|
MYT1
|
[NCBI]
|
3.42458e-05
|
|
|
MNGIE
|
[NCBI]
|
3.39456e-05
|
|
|
MDC1A
|
[NCBI]
|
3.32442e-05
|
|
|
GSD
|
[NCBI]
|
3.32442e-05
|
|
|
EAOH
|
[NCBI]
|
3.32442e-05
|
|
|
LITAF
|
[NCBI]
|
3.26028e-05
|
|
|
CXCL10
|
[NCBI]
|
3.26028e-05
|
|
|
GAN1
|
[NCBI]
|
3.1935e-05
|
|
|
SMA2
|
[NCBI]
|
3.13222e-05
|
|
|
RTN4
|
[NCBI]
|
3.11993e-05
|
|
|
BMP7
|
[NCBI]
|
3.11993e-05
|
|
|
DNM2
|
[NCBI]
|
3.11993e-05
|
|
|
PRPS1
|
[NCBI]
|
3.11993e-05
|
|
|
PRL
|
[NCBI]
|
3.11497e-05
|
|
|
KSS
|
[NCBI]
|
3.09059e-05
|
|
|
EGF
|
[NCBI]
|
2.91792e-05
|
|
|
ATRN
|
[NCBI]
|
2.88895e-05
|
|
|
NDRG1
|
[NCBI]
|
2.88895e-05
|
|
|
cerebrotendinous xanthomatosis
|
[NCBI]
|
2.85982e-05
|
|
|
AHC
|
[NCBI]
|
2.81109e-05
|
|
|
OPA1
|
[NCBI]
|
2.81109e-05
|
|
|
MST1
|
[NCBI]
|
2.79153e-05
|
|
|
megaloblastic anemia 1
|
[NCBI]
|
2.764e-05
|
|
|
MOG
|
[NCBI]
|
2.70318e-05
|
|
|
panencephalitis, subacute sclerosing
|
[NCBI]
|
2.68709e-05
|
|
|
TGD
|
[NCBI]
|
2.67433e-05
|
|
|
CD44
|
[NCBI]
|
2.62239e-05
|
|
|
mannosidosis, alpha b, lysosomal
|
[NCBI]
|
2.59013e-05
|
|
|
homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolate reductase activity
|
[NCBI]
|
2.59013e-05
|
|
|
CHAC
|
[NCBI]
|
2.59013e-05
|
|
|
ERCC3
|
[NCBI]
|
2.47907e-05
|
|
|
ATXN3
|
[NCBI]
|
2.47907e-05
|
|
|
LIFR
|
[NCBI]
|
2.35488e-05
|
|
|
EPO
|
[NCBI]
|
2.31652e-05
|
|
|
HSAN3
|
[NCBI]
|
2.20242e-05
|
|
|
CDG1A
|
[NCBI]
|
2.17223e-05
|
|
|
CNTF
|
[NCBI]
|
2.00407e-05
|
|
|
ABL
|
[NCBI]
|
1.85675e-05
|
|
|
IL3
|
[NCBI]
|
1.80509e-05
|
|
|
TLR3
|
[NCBI]
|
1.80509e-05
|
|
|
SOCS3
|
[NCBI]
|
1.74417e-05
|
|
|
BMP4
|
[NCBI]
|
1.74417e-05
|
|
|
ERBB2
|
[NCBI]
|
1.68727e-05
|
|
|
AMC
|
[NCBI]
|
1.68404e-05
|
|
|
DBI
|
[NCBI]
|
1.44905e-05
|
|
|
menkes disease
|
[NCBI]
|
1.37021e-05
|
|
|
LS
|
[NCBI]
|
1.28296e-05
|
|
|
IL4
|
[NCBI]
|
1.18674e-05
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
1.14875e-05
|
|
|
HGF
|
[NCBI]
|
1.11236e-05
|
|
|
wilson disease
|
[NCBI]
|
1.05913e-05
|
|
|
FRDA
|
[NCBI]
|
9.94883e-06
|
|
|
NGFR
|
[NCBI]
|
9.5871e-06
|
|
|
PNPLA6
|
[NCBI]
|
7.7899e-06
|
|
|
HPRT1
|
[NCBI]
|
7.16203e-06
|
|
|
DRPLA
|
[NCBI]
|
6.80219e-06
|
|
|
TF
|
[NCBI]
|
6.06797e-06
|
|
|
PLG
|
[NCBI]
|
4.72542e-06
|
|
|
G6PD
|
[NCBI]
|
3.92325e-06
|
|
|
AD
|
[NCBI]
|
2.81942e-06
|
|
|
GDNF
|
[NCBI]
|
2.81085e-06
|
|
|
PRNP
|
[NCBI]
|
2.64483e-06
|
|
|
INS
|
[NCBI]
|
2.48211e-06
|
|
|
CP
|
[NCBI]
|
2.06473e-06
|
|
|
MJD
|
[NCBI]
|
2.0615e-06
|
|
|
LCAT
|
[NCBI]
|
1.88863e-06
|
|
|
SOD1
|
[NCBI]
|
1.66558e-06
|
|
|
ACHE
|
[NCBI]
|
1.2316e-06
|
|
|
NGFB
|
[NCBI]
|
1.02991e-06
|
|
|
CJD
|
[NCBI]
|
9.63064e-07
|
|
|
MG
|
[NCBI]
|
7.28926e-07
|
|
|
BDNF
|
[NCBI]
|
4.77646e-07
|
|
|
SPP1
|
[NCBI]
|
4.4966e-07
|
|
|
MDD
|
[NCBI]
|
3.71084e-07
|
|
|
TNF
|
[NCBI]
|
2.26953e-07
|
|
|
APOB
|
[NCBI]
|
2.15821e-07
|
|