|
OMIM |
Link |
Information gain |
01 |
|
MBS
|
[NCBI]
|
0.00438177
|
|
|
KSS
|
[NCBI]
|
0.00322456
|
|
|
CFEOM3
|
[NCBI]
|
0.00270912
|
|
|
ophthalmoplegia, familial static
|
[NCBI]
|
0.00232341
|
|
|
DURS1
|
[NCBI]
|
0.00217033
|
|
|
visceral myopathy, familial, with external ophthalmoplegia
|
[NCBI]
|
0.00202422
|
|
|
DA5
|
[NCBI]
|
0.000996868
|
|
|
ocular myopathy with curare sensitivity
|
[NCBI]
|
0.000887234
|
|
|
CFEOM3B
|
[NCBI]
|
0.000887234
|
|
|
CFEOM3A
|
[NCBI]
|
0.000887234
|
|
|
CFEOM1
|
[NCBI]
|
0.000762923
|
|
|
OPEM
|
[NCBI]
|
0.000669824
|
|
|
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 1
|
[NCBI]
|
0.000613723
|
|
|
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 3
|
[NCBI]
|
0.000523885
|
|
|
MNGIE
|
[NCBI]
|
0.000497154
|
|
|
PSNP2
|
[NCBI]
|
0.000496053
|
|
|
SCAX1
|
[NCBI]
|
0.000439168
|
|
|
ocular motor apraxia
|
[NCBI]
|
0.00041718
|
|
|
visceral neuropathy, familial, autosomal recessive
|
[NCBI]
|
0.000398025
|
|
|
gordon syndrome
|
[NCBI]
|
0.000381069
|
|
|
RA
|
[NCBI]
|
0.000373833
|
|
|
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive
|
[NCBI]
|
0.000373445
|
|
|
fibrosis of extraocular muscles, congenital, with synergistic divergence
|
[NCBI]
|
0.000307869
|
|
|
wildervanck syndrome
|
[NCBI]
|
0.000287105
|
|
|
DRRS
|
[NCBI]
|
0.000256532
|
|
|
HGPPS
|
[NCBI]
|
0.000230491
|
|
|
optic atrophy 1 and deafness
|
[NCBI]
|
0.000230491
|
|
|
POLG
|
[NCBI]
|
0.00021982
|
|
|
NPC1
|
[NCBI]
|
0.000217823
|
|
|
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 2
|
[NCBI]
|
0.000215176
|
|
|
minicore myopathy with external ophthalmoplegia
|
[NCBI]
|
0.000209044
|
|
|
ophthalmoplegic neuromuscular disorder with abnormal mitochondria
|
[NCBI]
|
0.000205144
|
|
|
C10ORF2
|
[NCBI]
|
0.000199605
|
|
|
SCA7
|
[NCBI]
|
0.000177422
|
|
|
OPA1
|
[NCBI]
|
0.00017324
|
|
|
OPMD
|
[NCBI]
|
0.00017122
|
|
|
RYR1
|
[NCBI]
|
0.000139099
|
|
|
SLE
|
[NCBI]
|
0.000133095
|
|
|
IBM3
|
[NCBI]
|
0.00013239
|
|
|
SCCMS
|
[NCBI]
|
0.000103818
|
|
|
motor neuron disease with dementia and ophthalmoplegia
|
[NCBI]
|
0.000102521
|
|
|
oculopharyngodistal myopathy
|
[NCBI]
|
0.000102521
|
|
|
ophthalmoplegia, familial total, with iris transillumination
|
[NCBI]
|
0.000102521
|
|
|
ophthalmoplegia, progressive, with scrotal tongue and mental deficiency
|
[NCBI]
|
0.000102521
|
|
|
cranial nerves, recurrent paresis of
|
[NCBI]
|
0.000102521
|
|
|
schimke x-linked mental retardation syndrome
|
[NCBI]
|
0.000102521
|
|
|
KIF21A
|
[NCBI]
|
8.63527e-05
|
|
|
mental retardation, x-linked, south african type
|
[NCBI]
|
8.63527e-05
|
|
|
MJD
|
[NCBI]
|
8.27475e-05
|
|
|
MTTL1
|
[NCBI]
|
8.00232e-05
|
|
|
PEOA4
|
[NCBI]
|
7.1624e-05
|
|
|
ROBO3
|
[NCBI]
|
6.73738e-05
|
|
|
spastic ataxia
|
[NCBI]
|
6.61447e-05
|
|
|
paroxysmal tonic upgaze, benign childhood, with ataxia
|
[NCBI]
|
6.61447e-05
|
|
|
CFEOM2
|
[NCBI]
|
6.61447e-05
|
|
|
ivic syndrome
|
[NCBI]
|
6.61447e-05
|
|
|
FSHMD1A
|
[NCBI]
|
6.56598e-05
|
|
|
MTTW
|
[NCBI]
|
6.14875e-05
|
|
|
MTND2
|
[NCBI]
|
5.94876e-05
|
|
|
SCA2
|
[NCBI]
|
5.61651e-05
|
|
|
SANDO
|
[NCBI]
|
5.61572e-05
|
|
|
mitochondrial complex ii deficiency
|
[NCBI]
|
5.61572e-05
|
|
|
myopathy, centronuclear, autosomal recessive
|
[NCBI]
|
5.61572e-05
|
|
|
mitochondrial myopathy with diabetes
|
[NCBI]
|
5.38624e-05
|
|
|
myopathy, centronuclear, autosomal dominant
|
[NCBI]
|
5.38624e-05
|
|
|
MG
|
[NCBI]
|
5.37063e-05
|
|
|
GLUD1
|
[NCBI]
|
5.05631e-05
|
|
|
ATXN2
|
[NCBI]
|
5.05631e-05
|
|
|
SALL4
|
[NCBI]
|
4.91925e-05
|
|
|
SCA1
|
[NCBI]
|
4.90407e-05
|
|
|
spinocerebellar ataxia, 16q22-linked
|
[NCBI]
|
4.84891e-05
|
|
|
mitochondrial dna depletion syndrome, myopathic form
|
[NCBI]
|
4.44997e-05
|
|
|
NPC1
|
[NCBI]
|
4.28169e-05
|
|
|
mitochondrial dna depletion syndrome, hepatocerebral form
|
[NCBI]
|
4.23173e-05
|
|
|
pearson marrow-pancreas syndrome
|
[NCBI]
|
4.13324e-05
|
|
|
myasthenic syndrome, congenital, associated with episodic apnea
|
[NCBI]
|
4.13324e-05
|
|
|
DLB
|
[NCBI]
|
3.79288e-05
|
|
|
EAOH
|
[NCBI]
|
3.64775e-05
|
|
|
niemann-pick disease, type b
|
[NCBI]
|
3.51548e-05
|
|
|
PSNP1
|
[NCBI]
|
3.45352e-05
|
|
|
MELAS
|
[NCBI]
|
3.39405e-05
|
|
|
LCA1
|
[NCBI]
|
3.17774e-05
|
|
|
MSS
|
[NCBI]
|
3.12834e-05
|
|
|
OPA1
|
[NCBI]
|
3.12834e-05
|
|
|
RSMD1
|
[NCBI]
|
2.98955e-05
|
|
|
maple syrup urine disease
|
[NCBI]
|
2.06222e-05
|
|
|
AMC
|
[NCBI]
|
1.97628e-05
|
|
|
TTR
|
[NCBI]
|
1.41059e-05
|
|
|
HD
|
[NCBI]
|
1.30354e-05
|
|
|
temporal arteritis
|
[NCBI]
|
9.50438e-06
|
|
|
TSD
|
[NCBI]
|
6.61262e-06
|
|
|
CJD
|
[NCBI]
|
4.92296e-06
|
|