|
OMIM |
Link |
Information gain |
01 |
|
myopathy with deficiency of succinate dehydrogenase and aconitase
|
[NCBI]
|
0.00168774
|
|
|
WDM
|
[NCBI]
|
0.00168774
|
|
|
carnitine deficiency, myopathic
|
[NCBI]
|
0.00154489
|
|
|
muscular dystrophy, congenital, megaconial type
|
[NCBI]
|
0.000213124
|
|
|
IBM3
|
[NCBI]
|
0.000151528
|
|
|
tibial muscular dystrophy, tardive
|
[NCBI]
|
0.00014445
|
|
|
MSS
|
[NCBI]
|
0.000134706
|
|
|
danon disease
|
[NCBI]
|
0.000125145
|
|
|
leber optic atrophy
|
[NCBI]
|
7.42093e-05
|
|
|
MUC15
|
[NCBI]
|
5.04133e-05
|
|
|
MYH2
|
[NCBI]
|
4.24643e-05
|
|
|
LAMP2
|
[NCBI]
|
3.68597e-05
|
|
|
UTRN
|
[NCBI]
|
3.68597e-05
|
|
|
DMD
|
[NCBI]
|
2.42237e-05
|
|
|
TH
|
[NCBI]
|
8.42562e-06
|
|
|
ACHE
|
[NCBI]
|
7.94985e-06
|
|