|
OMIM |
Link |
Information gain |
01 |
|
MBS
|
[NCBI]
|
0.014579
|
|
|
HCFP1
|
[NCBI]
|
0.00432406
|
|
|
HCFP2
|
[NCBI]
|
0.00258184
|
|
|
facial palsy, familial recurrent peripheral
|
[NCBI]
|
0.00258184
|
|
|
cayler cardiofacial syndrome
|
[NCBI]
|
0.00248043
|
|
|
johnson neuroectodermal syndrome
|
[NCBI]
|
0.00128253
|
|
|
bulbar palsy, progressive, with sensorineural deafness
|
[NCBI]
|
0.000465865
|
|
|
OSCS
|
[NCBI]
|
0.00029888
|
|
|
HFM
|
[NCBI]
|
0.00029781
|
|
|
BPP
|
[NCBI]
|
0.000178142
|
|
|
poland syndrome
|
[NCBI]
|
0.000169384
|
|
|
amyloidosis v
|
[NCBI]
|
0.000157517
|
|
|
CMDD
|
[NCBI]
|
0.000152259
|
|
|
charge syndrome
|
[NCBI]
|
0.000132394
|
|
|
oculopharyngodistal myopathy
|
[NCBI]
|
0.000129339
|
|
|
deafness, conductive stapedial, with ear malformation and facial palsy
|
[NCBI]
|
0.000129339
|
|
|
ophthalmoplegia, progressive, with scrotal tongue and mental deficiency
|
[NCBI]
|
0.000129339
|
|
|
cranial nerves, recurrent paresis of
|
[NCBI]
|
0.000129339
|
|
|
NF2
|
[NCBI]
|
0.000115273
|
|
|
ophthalmoplegic neuromuscular disorder with abnormal mitochondria
|
[NCBI]
|
0.000106872
|
|
|
pachygyria with mental retardation and seizures
|
[NCBI]
|
9.28923e-05
|
|
|
SOX14
|
[NCBI]
|
8.42364e-05
|
|
|
hyperostosis corticalis generalisata, benign form of worth, with torus palatinus
|
[NCBI]
|
7.66903e-05
|
|
|
lenz-majewski hyperostotic dwarfism
|
[NCBI]
|
7.66903e-05
|
|
|
wildervanck syndrome
|
[NCBI]
|
7.36018e-05
|
|
|
hyperostosis corticalis generalisata
|
[NCBI]
|
7.36018e-05
|
|
|
OPTA2
|
[NCBI]
|
7.10121e-05
|
|
|
GSN
|
[NCBI]
|
5.86805e-05
|
|
|
HYPP
|
[NCBI]
|
5.18422e-05
|
|
|
FSHMD1A
|
[NCBI]
|
4.64892e-05
|
|
|
OCP
|
[NCBI]
|
4.36525e-05
|
|
|
SDC2
|
[NCBI]
|
4.35421e-05
|
|
|
OPMD
|
[NCBI]
|
3.45196e-05
|
|
|
SOD2
|
[NCBI]
|
3.4423e-05
|
|
|
KSS
|
[NCBI]
|
3.24666e-05
|
|
|
DGS
|
[NCBI]
|
2.98032e-05
|
|
|
dystrophia myotonica 1
|
[NCBI]
|
2.59404e-05
|
|
|
MBP
|
[NCBI]
|
2.04944e-05
|
|
|
panencephalitis, subacute sclerosing
|
[NCBI]
|
1.22245e-05
|
|
|
lymphoma, non-hodgkin, familial
|
[NCBI]
|
9.31249e-06
|
|
|
SLE
|
[NCBI]
|
1.39142e-06
|
|