|
OMIM |
Link |
Information gain |
01 |
|
rhabdomyolysis, acute recurrent
|
[NCBI]
|
0.00102023
|
|
|
myopathy with deficiency of succinate dehydrogenase and aconitase
|
[NCBI]
|
0.00092257
|
|
|
MB
|
[NCBI]
|
0.000310055
|
|
|
trifunctional protein deficiency
|
[NCBI]
|
0.000194088
|
|
|
carnitine palmitoyltransferase ii deficiency, late-onset
|
[NCBI]
|
0.00017017
|
|
|
BMD
|
[NCBI]
|
0.000147749
|
|
|
ACADS
|
[NCBI]
|
0.000111573
|
|
|
PGK1
|
[NCBI]
|
0.000102132
|
|
|
CYP2C8
|
[NCBI]
|
8.96982e-05
|
|
|
brody myopathy
|
[NCBI]
|
8.76406e-05
|
|
|
congenital cataracts, facial dysmorphism, and neuropathy
|
[NCBI]
|
8.31968e-05
|
|
|
phosphoglycerate kinase 1 deficiency
|
[NCBI]
|
8.19513e-05
|
|
|
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 1
|
[NCBI]
|
7.68556e-05
|
|
|
myopathy, myofibrillar, desmin-related
|
[NCBI]
|
7.10508e-05
|
|
|
MSS
|
[NCBI]
|
6.82623e-05
|
|
|
MADD
|
[NCBI]
|
6.82623e-05
|
|
|
DM2
|
[NCBI]
|
6.00385e-05
|
|
|
MHS1
|
[NCBI]
|
5.77611e-05
|
|
|
IVD
|
[NCBI]
|
5.54947e-05
|
|
|
LDHA
|
[NCBI]
|
5.54947e-05
|
|
|
CPT2
|
[NCBI]
|
5.46665e-05
|
|
|
ACADVL
|
[NCBI]
|
5.39023e-05
|
|
|
ACADM
|
[NCBI]
|
3.52958e-05
|
|
|
SPINK1
|
[NCBI]
|
2.97708e-05
|
|
|
DMD
|
[NCBI]
|
2.77427e-05
|
|
|
G6PD
|
[NCBI]
|
1.22618e-05
|
|
|
CAT
|
[NCBI]
|
1.10553e-05
|
|
|
SLE
|
[NCBI]
|
2.7341e-08
|
|