|
OMIM |
Link |
Information gain |
01 |
|
myositis
|
[NCBI]
|
0.00123814
|
|
|
inclusion body myositis
|
[NCBI]
|
0.000787083
|
|
|
APS2
|
[NCBI]
|
0.000697531
|
|
|
scleroderma, familial progressive
|
[NCBI]
|
0.00058575
|
|
|
SLE
|
[NCBI]
|
0.000465524
|
|
|
OPMD
|
[NCBI]
|
0.000176312
|
|
|
TTN
|
[NCBI]
|
0.000167567
|
|
|
MG
|
[NCBI]
|
0.000141458
|
|
|
NM
|
[NCBI]
|
0.000139754
|
|
|
IBM2
|
[NCBI]
|
0.000125855
|
|
|
CAPN3
|
[NCBI]
|
9.44138e-05
|
|
|
EXOSC9
|
[NCBI]
|
8.35435e-05
|
|
|
BTK
|
[NCBI]
|
7.09595e-05
|
|
|
KARS
|
[NCBI]
|
6.9765e-05
|
|
|
mitochondrial dna depletion syndrome, hepatocerebral form
|
[NCBI]
|
5.57698e-05
|
|
|
EDMD2
|
[NCBI]
|
5.05385e-05
|
|
|
myopathy, myofibrillar, desmin-related
|
[NCBI]
|
4.72104e-05
|
|
|
central core disease of muscle
|
[NCBI]
|
4.60556e-05
|
|
|
LGMD2A
|
[NCBI]
|
4.21438e-05
|
|
|
periodic fever, familial, autosomal dominant
|
[NCBI]
|
4.21438e-05
|
|
|
TNF
|
[NCBI]
|
3.96516e-05
|
|
|
TNFRSF1A
|
[NCBI]
|
3.47254e-05
|
|
|
GPT
|
[NCBI]
|
3.41583e-05
|
|
|
STAT1
|
[NCBI]
|
3.26324e-05
|
|
|
AMC
|
[NCBI]
|
3.23353e-05
|
|
|
MB
|
[NCBI]
|
2.61536e-05
|
|
|
AGER
|
[NCBI]
|
2.5463e-05
|
|
|
APP
|
[NCBI]
|
2.35318e-05
|
|
|
COMP
|
[NCBI]
|
2.19349e-05
|
|
|
CNTF
|
[NCBI]
|
1.66093e-05
|
|
|
ACP5
|
[NCBI]
|
1.5232e-05
|
|
|
RA
|
[NCBI]
|
1.37965e-05
|
|
|
MPO
|
[NCBI]
|
1.25854e-05
|
|
|
CVID
|
[NCBI]
|
9.64814e-06
|
|
|
RNASE3
|
[NCBI]
|
8.36605e-06
|
|
|
TNFSF6
|
[NCBI]
|
7.87669e-06
|
|
|
ACHE
|
[NCBI]
|
5.26212e-06
|
|
|
APOE
|
[NCBI]
|
2.59429e-06
|
|
|
GFAP
|
[NCBI]
|
2.02163e-06
|
|
|
VEGF
|
[NCBI]
|
1.95792e-06
|
|
|
NGFB
|
[NCBI]
|
1.74147e-06
|
|
|
PTH
|
[NCBI]
|
8.56464e-08
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
2.87941e-08
|
|