|
OMIM |
Link |
Information gain |
01 |
|
CFEOM3
|
[NCBI]
|
0.00860956
|
|
|
OPMD
|
[NCBI]
|
0.00602572
|
|
|
CFEOM1
|
[NCBI]
|
0.00186219
|
|
|
duane retraction syndrome 2
|
[NCBI]
|
0.00173626
|
|
|
strabismus, susceptibility to
|
[NCBI]
|
0.00173626
|
|
|
MG
|
[NCBI]
|
0.00137932
|
|
|
tukel syndrome
|
[NCBI]
|
0.00128958
|
|
|
OPEM
|
[NCBI]
|
0.00128958
|
|
|
CFEOM3B
|
[NCBI]
|
0.00128958
|
|
|
CFEOM3A
|
[NCBI]
|
0.00128958
|
|
|
wieacker syndrome
|
[NCBI]
|
0.000862604
|
|
|
ocular motor apraxia
|
[NCBI]
|
0.000787075
|
|
|
inclusion body myositis
|
[NCBI]
|
0.00068662
|
|
|
NNO1
|
[NCBI]
|
0.00068662
|
|
|
fibrosis of extraocular muscles, congenital, with synergistic divergence
|
[NCBI]
|
0.000515349
|
|
|
CFEOM2
|
[NCBI]
|
0.000515349
|
|
|
RA
|
[NCBI]
|
0.000398248
|
|
|
MBS
|
[NCBI]
|
0.000382199
|
|
|
SPS
|
[NCBI]
|
0.000382199
|
|
|
EAOH
|
[NCBI]
|
0.000303466
|
|
|
KSS
|
[NCBI]
|
0.000208618
|
|
|
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive
|
[NCBI]
|
0.00019615
|
|
|
vestibulocochlear dysfunction, progressive
|
[NCBI]
|
0.000171545
|
|
|
ophthalmoplegia, familial total, with iris transillumination
|
[NCBI]
|
0.000171545
|
|
|
MYH13
|
[NCBI]
|
0.000163021
|
|
|
camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye
|
[NCBI]
|
0.000132334
|
|
|
APTX
|
[NCBI]
|
0.000128864
|
|
|
SLE
|
[NCBI]
|
0.000112933
|
|
|
gaucher disease, type iiic
|
[NCBI]
|
0.000108014
|
|
|
axenfeld-rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities
|
[NCBI]
|
0.000108014
|
|
|
PABPN1
|
[NCBI]
|
9.22345e-05
|
|
|
SPMM
|
[NCBI]
|
9.06051e-05
|
|
|
minicore myopathy with external ophthalmoplegia
|
[NCBI]
|
8.31255e-05
|
|
|
MNGIE
|
[NCBI]
|
7.03398e-05
|
|
|
EA2
|
[NCBI]
|
6.83807e-05
|
|
|
graves disease
|
[NCBI]
|
6.65567e-05
|
|
|
DLB
|
[NCBI]
|
6.32498e-05
|
|
|
ACHE
|
[NCBI]
|
6.17702e-05
|
|
|
SCA6
|
[NCBI]
|
5.31118e-05
|
|
|
KIF21A
|
[NCBI]
|
5.22273e-05
|
|
|
SJS1
|
[NCBI]
|
5.01591e-05
|
|
|
SCA2
|
[NCBI]
|
4.36795e-05
|
|
|
MTM1
|
[NCBI]
|
3.39734e-05
|
|
|
MTM1
|
[NCBI]
|
3.20029e-05
|
|
|
ICAM1
|
[NCBI]
|
3.09187e-05
|
|
|
FN1
|
[NCBI]
|
3.06715e-05
|
|
|
SCA1
|
[NCBI]
|
3.05559e-05
|
|
|
GBA
|
[NCBI]
|
2.75708e-05
|
|
|
TG
|
[NCBI]
|
2.61917e-05
|
|
|
CHAT
|
[NCBI]
|
2.6055e-05
|
|
|
RYR1
|
[NCBI]
|
2.57772e-05
|
|
|
GDNF
|
[NCBI]
|
2.23774e-05
|
|
|
RHO
|
[NCBI]
|
2.22942e-05
|
|
|
DMD
|
[NCBI]
|
1.97734e-05
|
|
|
NF1
|
[NCBI]
|
1.78553e-05
|
|
|
SST
|
[NCBI]
|
1.75143e-05
|
|
|
SLC18A3
|
[NCBI]
|
1.72251e-05
|
|
|
DMD
|
[NCBI]
|
1.3673e-05
|
|
|
dystrophia myotonica 1
|
[NCBI]
|
1.33783e-05
|
|
|
GAL
|
[NCBI]
|
1.1659e-05
|
|
|
MJD
|
[NCBI]
|
1.07526e-05
|
|
|
PD
|
[NCBI]
|
8.82225e-06
|
|
|
NPY
|
[NCBI]
|
5.00111e-06
|
|
|
TNFSF6
|
[NCBI]
|
4.95005e-06
|
|
|
HGF
|
[NCBI]
|
2.27965e-06
|
|
|
BDNF
|
[NCBI]
|
1.37696e-06
|
|
|
VIP
|
[NCBI]
|
1.03749e-06
|
|
|
VEGF
|
[NCBI]
|
5.29462e-07
|
|
|
RP
|
[NCBI]
|
1.25127e-08
|
|