|
OMIM |
Link |
Information gain |
01 |
|
WDM
|
[NCBI]
|
0.00201127
|
|
|
myopathy, distal, with onset in infancy
|
[NCBI]
|
0.00154746
|
|
|
NEM3
|
[NCBI]
|
0.00133097
|
|
|
NEM6
|
[NCBI]
|
0.00123667
|
|
|
myopathy, hyaline body, autosomal recessive
|
[NCBI]
|
0.0011195
|
|
|
carnitine deficiency, myopathic
|
[NCBI]
|
0.000844839
|
|
|
NLS
|
[NCBI]
|
0.000711442
|
|
|
MTM1
|
[NCBI]
|
0.000460406
|
|
|
RSMD1
|
[NCBI]
|
0.00042361
|
|
|
CD
|
[NCBI]
|
0.000422141
|
|
|
myopathy, centronuclear, autosomal dominant
|
[NCBI]
|
0.000421833
|
|
|
myopathy with storage of glycoproteins and glycosaminoglycans
|
[NCBI]
|
0.000316957
|
|
|
central core disease of muscle
|
[NCBI]
|
0.000294579
|
|
|
cardiomyopathy, infantile histiocytoid
|
[NCBI]
|
0.000262975
|
|
|
LGMD1A
|
[NCBI]
|
0.000252566
|
|
|
myopathy, myosin storage
|
[NCBI]
|
0.000229563
|
|
|
tibial muscular dystrophy, tardive
|
[NCBI]
|
0.000204658
|
|
|
CFTD
|
[NCBI]
|
0.00019716
|
|
|
dystonia with ringbinden
|
[NCBI]
|
0.000185316
|
|
|
NEM7
|
[NCBI]
|
0.000185316
|
|
|
myopathy, myofibrillar, desmin-related
|
[NCBI]
|
0.00017221
|
|
|
TMOD
|
[NCBI]
|
0.000163656
|
|
|
pleoconial myopathy with salt craving
|
[NCBI]
|
0.000146079
|
|
|
filaminopathy, autosomal dominant
|
[NCBI]
|
0.000146079
|
|
|
ophthalmoplegic neuromuscular disorder with abnormal mitochondria
|
[NCBI]
|
0.000146079
|
|
|
myopathy with giant abnormal mitochondria
|
[NCBI]
|
0.000131295
|
|
|
alpha-b crystallinopathy
|
[NCBI]
|
0.000121708
|
|
|
spinal muscular atrophy, proximal, adult, autosomal dominant
|
[NCBI]
|
0.00011459
|
|
|
DES
|
[NCBI]
|
0.000104366
|
|
|
mitochondrial myopathy
|
[NCBI]
|
9.6691e-05
|
|
|
KSS
|
[NCBI]
|
9.26123e-05
|
|
|
myotonia congenita, autosomal dominant
|
[NCBI]
|
9.07797e-05
|
|
|
LGMD2D
|
[NCBI]
|
9.07797e-05
|
|
|
COFS1
|
[NCBI]
|
8.37771e-05
|
|
|
DMD
|
[NCBI]
|
8.25962e-05
|
|
|
UCMD
|
[NCBI]
|
8.17922e-05
|
|
|
SMA3
|
[NCBI]
|
8.17922e-05
|
|
|
abdominal muscles, absence of, with urinary tract abnormality and cryptorchidism
|
[NCBI]
|
7.82114e-05
|
|
|
CF
|
[NCBI]
|
7.39516e-05
|
|
|
HYPP
|
[NCBI]
|
6.84743e-05
|
|
|
glycogen storage disease v
|
[NCBI]
|
6.62411e-05
|
|
|
SJS1
|
[NCBI]
|
6.32115e-05
|
|
|
CMT1B
|
[NCBI]
|
5.44106e-05
|
|
|
RSTS
|
[NCBI]
|
5.44106e-05
|
|
|
EDMD
|
[NCBI]
|
5.00726e-05
|
|
|
CACNB1
|
[NCBI]
|
4.60671e-05
|
|
|
TRIM32
|
[NCBI]
|
4.36217e-05
|
|
|
CFL2
|
[NCBI]
|
4.18038e-05
|
|
|
glycogen storage disease ii
|
[NCBI]
|
4.07502e-05
|
|
|
ADSS
|
[NCBI]
|
4.03555e-05
|
|
|
FLNC
|
[NCBI]
|
3.91513e-05
|
|
|
TTID
|
[NCBI]
|
3.91513e-05
|
|
|
SEPN1
|
[NCBI]
|
3.91513e-05
|
|
|
BCAR1
|
[NCBI]
|
3.64199e-05
|
|
|
SLE
|
[NCBI]
|
3.54153e-05
|
|
|
SGCA
|
[NCBI]
|
3.50464e-05
|
|
|
RYR3
|
[NCBI]
|
3.50464e-05
|
|
|
CMH
|
[NCBI]
|
3.41145e-05
|
|
|
ACTC1
|
[NCBI]
|
3.33815e-05
|
|
|
PTK2
|
[NCBI]
|
3.11085e-05
|
|
|
CLCN1
|
[NCBI]
|
2.96207e-05
|
|
|
CRYAB
|
[NCBI]
|
2.96207e-05
|
|
|
MTM1
|
[NCBI]
|
2.96207e-05
|
|
|
MSTN
|
[NCBI]
|
2.67707e-05
|
|
|
RUNX1
|
[NCBI]
|
2.67707e-05
|
|
|
CSF3
|
[NCBI]
|
2.639e-05
|
|
|
DSTN
|
[NCBI]
|
2.62071e-05
|
|
|
BIRC1
|
[NCBI]
|
2.50444e-05
|
|
|
RYR1
|
[NCBI]
|
2.34122e-05
|
|
|
AQP4
|
[NCBI]
|
2.30573e-05
|
|
|
GAPDH
|
[NCBI]
|
2.30274e-05
|
|
|
UCP3
|
[NCBI]
|
2.14201e-05
|
|
|
FGF2
|
[NCBI]
|
1.69088e-05
|
|
|
GPI
|
[NCBI]
|
1.52148e-05
|
|
|
MB
|
[NCBI]
|
1.42983e-05
|
|
|
PDCD8
|
[NCBI]
|
1.29861e-05
|
|
|
IAPP
|
[NCBI]
|
1.29348e-05
|
|
|
NPPA
|
[NCBI]
|
1.26433e-05
|
|
|
SRF
|
[NCBI]
|
9.86124e-06
|
|
|
XDH
|
[NCBI]
|
7.31896e-06
|
|
|
RNASE3
|
[NCBI]
|
5.78795e-06
|
|
|
ACHE
|
[NCBI]
|
3.88513e-06
|
|
|
TNF
|
[NCBI]
|
1.1003e-06
|
|
|
HGF
|
[NCBI]
|
1.02091e-06
|
|
|
MG
|
[NCBI]
|
6.36224e-07
|
|
|
PCNA
|
[NCBI]
|
5.6791e-07
|
|