|
OMIM |
Link |
Information gain |
01 |
|
SMAX1
|
[NCBI]
|
0.00796804
|
|
|
SMA1
|
[NCBI]
|
0.00417458
|
|
|
SMN1
|
[NCBI]
|
0.00395637
|
|
|
amyotrophy, monomelic
|
[NCBI]
|
0.00286521
|
|
|
SMA2
|
[NCBI]
|
0.00189185
|
|
|
SMN2
|
[NCBI]
|
0.00179251
|
|
|
AR
|
[NCBI]
|
0.00167309
|
|
|
SMA3
|
[NCBI]
|
0.00159686
|
|
|
DSMA3
|
[NCBI]
|
0.00150808
|
|
|
spinal muscular atrophy, distal, congenital nonprogressive
|
[NCBI]
|
0.00150808
|
|
|
amyotrophy, neurogenic scapuloperoneal, new england type
|
[NCBI]
|
0.00141524
|
|
|
BIRC1
|
[NCBI]
|
0.00141305
|
|
|
HMN7A
|
[NCBI]
|
0.00128649
|
|
|
spinal muscular atrophy, childhood, proximal, autosomal dominant
|
[NCBI]
|
0.0011591
|
|
|
spinal muscular atrophy, distal, x-linked recessive
|
[NCBI]
|
0.00096756
|
|
|
SMA4
|
[NCBI]
|
0.000810024
|
|
|
spinal muscular atrophy, facioscapulohumeral type
|
[NCBI]
|
0.000614885
|
|
|
arthrogryposis multiplex congenita, distal, x-linked
|
[NCBI]
|
0.000614885
|
|
|
charcot-marie-tooth disease, dominant intermediate a
|
[NCBI]
|
0.000614885
|
|
|
hereditary motor and sensory neuropathy, type iic
|
[NCBI]
|
0.000544153
|
|
|
lethal congenital contracture syndrome 1
|
[NCBI]
|
0.000544153
|
|
|
SIP1
|
[NCBI]
|
0.00042194
|
|
|
DSMA1
|
[NCBI]
|
0.000341687
|
|
|
HMN5
|
[NCBI]
|
0.000261299
|
|
|
GARS
|
[NCBI]
|
0.000247299
|
|
|
pena-shokeir syndrome, type i
|
[NCBI]
|
0.000245071
|
|
|
CMT1A
|
[NCBI]
|
0.000207582
|
|
|
spinal muscular atrophy, proximal, adult, autosomal dominant
|
[NCBI]
|
0.000204766
|
|
|
CMT2D
|
[NCBI]
|
0.000204766
|
|
|
SFRS10
|
[NCBI]
|
0.00017105
|
|
|
DRPLA
|
[NCBI]
|
0.000143824
|
|
|
IGHMBP2
|
[NCBI]
|
0.000136539
|
|
|
SFRS9
|
[NCBI]
|
0.000128885
|
|
|
SERF1A
|
[NCBI]
|
0.000128885
|
|
|
GTF2H2
|
[NCBI]
|
0.000128885
|
|
|
FSHMD1A
|
[NCBI]
|
0.000124652
|
|
|
scapuloperoneal syndrome, neurogenic, kaeser type
|
[NCBI]
|
0.000117363
|
|
|
MAP1B
|
[NCBI]
|
0.000111257
|
|
|
CDH12
|
[NCBI]
|
0.000101354
|
|
|
radiation sensitivity/chromosome instability syndrome, autosomal dominant
|
[NCBI]
|
9.90568e-05
|
|
|
charcot-marie-tooth disease with ptosis and parkinsonism
|
[NCBI]
|
9.90568e-05
|
|
|
VEGF
|
[NCBI]
|
8.55078e-05
|
|
|
CMTX1
|
[NCBI]
|
7.41982e-05
|
|
|
keratosis pilaris
|
[NCBI]
|
6.81738e-05
|
|
|
ALS8
|
[NCBI]
|
6.81738e-05
|
|
|
tay-sachs disease, ab variant
|
[NCBI]
|
6.67103e-05
|
|
|
LIX1
|
[NCBI]
|
6.44203e-05
|
|
|
GEMIN4
|
[NCBI]
|
6.44203e-05
|
|
|
HNRPR
|
[NCBI]
|
6.44203e-05
|
|
|
SERF2
|
[NCBI]
|
6.44203e-05
|
|
|
DDX20
|
[NCBI]
|
6.44203e-05
|
|
|
CMT1B
|
[NCBI]
|
5.97084e-05
|
|
|
REN
|
[NCBI]
|
5.49701e-05
|
|
|
ZNF259
|
[NCBI]
|
5.06548e-05
|
|
|
RBMX
|
[NCBI]
|
5.06548e-05
|
|
|
ALS1
|
[NCBI]
|
4.86351e-05
|
|
|
HMN2A
|
[NCBI]
|
4.66822e-05
|
|
|
BIRC2
|
[NCBI]
|
4.54685e-05
|
|
|
RAB1
|
[NCBI]
|
4.54685e-05
|
|
|
RNR1
|
[NCBI]
|
4.54685e-05
|
|
|
LGMD1B
|
[NCBI]
|
4.2338e-05
|
|
|
CTF1
|
[NCBI]
|
4.21059e-05
|
|
|
CCNB1
|
[NCBI]
|
4.21059e-05
|
|
|
VAPB
|
[NCBI]
|
4.21059e-05
|
|
|
mitochondrial dna depletion syndrome, myopathic form
|
[NCBI]
|
4.11257e-05
|
|
|
MJD
|
[NCBI]
|
4.10681e-05
|
|
|
mowat-wilson syndrome
|
[NCBI]
|
4.00028e-05
|
|
|
CFTD
|
[NCBI]
|
3.79793e-05
|
|
|
TK2
|
[NCBI]
|
3.7623e-05
|
|
|
BIRC4
|
[NCBI]
|
3.7623e-05
|
|
|
BIRC3
|
[NCBI]
|
3.59737e-05
|
|
|
SPTLC1
|
[NCBI]
|
3.33333e-05
|
|
|
HSAN1
|
[NCBI]
|
3.31659e-05
|
|
|
ANKRD1
|
[NCBI]
|
3.03715e-05
|
|
|
ATF6
|
[NCBI]
|
2.81117e-05
|
|
|
ZEB2
|
[NCBI]
|
2.81117e-05
|
|
|
AIS
|
[NCBI]
|
2.67269e-05
|
|
|
TBP
|
[NCBI]
|
2.38647e-05
|
|
|
FY
|
[NCBI]
|
2.34476e-05
|
|
|
NEM3
|
[NCBI]
|
2.22595e-05
|
|
|
CAPN3
|
[NCBI]
|
2.12782e-05
|
|
|
CREBBP
|
[NCBI]
|
2.0962e-05
|
|
|
prostate cancer
|
[NCBI]
|
1.87304e-05
|
|
|
SPTA1
|
[NCBI]
|
1.50697e-05
|
|
|
RNASE2
|
[NCBI]
|
1.4462e-05
|
|
|
alopecia, androgenetic
|
[NCBI]
|
1.29043e-05
|
|
|
HD
|
[NCBI]
|
1.28737e-05
|
|
|
NGFB
|
[NCBI]
|
1.27775e-05
|
|
|
GFAP
|
[NCBI]
|
1.13908e-05
|
|
|
ACADM
|
[NCBI]
|
1.1255e-05
|
|
|
SMS
|
[NCBI]
|
1.10999e-05
|
|
|
LMNA
|
[NCBI]
|
1.06943e-05
|
|
|
FRDA
|
[NCBI]
|
9.88773e-06
|
|
|
CDK5
|
[NCBI]
|
9.84664e-06
|
|
|
BBS
|
[NCBI]
|
8.82082e-06
|
|
|
MG
|
[NCBI]
|
5.94706e-06
|
|
|
HGF
|
[NCBI]
|
4.95216e-06
|
|
|
TSD
|
[NCBI]
|
4.48156e-06
|
|
|
SOD1
|
[NCBI]
|
3.55526e-06
|
|
|
dystrophia myotonica 1
|
[NCBI]
|
2.79465e-06
|
|
|
GAPDH
|
[NCBI]
|
1.87487e-06
|
|
|
CNTF
|
[NCBI]
|
1.81556e-06
|
|
|
CFTR
|
[NCBI]
|
1.68819e-06
|
|
|
panencephalitis, subacute sclerosing
|
[NCBI]
|
9.84261e-07
|
|
|
AT
|
[NCBI]
|
7.0463e-07
|
|
|
ACHE
|
[NCBI]
|
1.27594e-09
|
|