|
OMIM |
Link |
Information gain |
01 |
|
myopathy, tubular aggregate
|
[NCBI]
|
0.00182258
|
|
|
CFTD2
|
[NCBI]
|
0.00123814
|
|
|
MTM1
|
[NCBI]
|
0.00103745
|
|
|
MTM1
|
[NCBI]
|
0.000955635
|
|
|
myasthenia, limb-girdle, with tubular aggregates
|
[NCBI]
|
0.000813359
|
|
|
CFTD
|
[NCBI]
|
0.000620715
|
|
|
DNM2
|
[NCBI]
|
0.000287968
|
|
|
ACTA1
|
[NCBI]
|
0.000196019
|
|
|
myopathy, centronuclear, autosomal recessive
|
[NCBI]
|
0.000195994
|
|
|
central core disease of muscle
|
[NCBI]
|
0.000146007
|
|
|
myasthenia, limb-girdle, autoimmune
|
[NCBI]
|
0.000100673
|
|
|
MTMR14
|
[NCBI]
|
8.52043e-05
|
|
|
myopathy, centronuclear, autosomal dominant
|
[NCBI]
|
8.279e-05
|
|
|
minicore myopathy with external ophthalmoplegia
|
[NCBI]
|
7.89629e-05
|
|
|
MTMR9
|
[NCBI]
|
7.14254e-05
|
|
|
CXORF6
|
[NCBI]
|
6.28498e-05
|
|
|
MTMR1
|
[NCBI]
|
6.03399e-05
|
|
|
LDB3
|
[NCBI]
|
5.83402e-05
|
|
|
DA2A
|
[NCBI]
|
5.81682e-05
|
|
|
SKI
|
[NCBI]
|
5.66775e-05
|
|
|
SEPN1
|
[NCBI]
|
5.66775e-05
|
|
|
SJS1
|
[NCBI]
|
5.37337e-05
|
|
|
costello syndrome
|
[NCBI]
|
5.11459e-05
|
|
|
ANKRD1
|
[NCBI]
|
5.10084e-05
|
|
|
glycogen storage disease ii
|
[NCBI]
|
4.26264e-05
|
|
|
DES
|
[NCBI]
|
3.9845e-05
|
|
|
HRAS
|
[NCBI]
|
3.69723e-05
|
|
|
AR
|
[NCBI]
|
4.1218e-06
|
|