|
OMIM |
Link |
Information gain |
01 |
|
DFNA16
|
[NCBI]
|
0.0015153
|
|
|
facial palsy, familial recurrent peripheral
|
[NCBI]
|
0.0015153
|
|
|
HFM
|
[NCBI]
|
0.00114649
|
|
|
deafness, progressive high-tone neural
|
[NCBI]
|
0.00108741
|
|
|
vestibulopathy, familial
|
[NCBI]
|
0.00101143
|
|
|
EVA
|
[NCBI]
|
0.000529532
|
|
|
alport syndrome, autosomal dominant
|
[NCBI]
|
0.000511298
|
|
|
klippel-trenaunay-weber syndrome
|
[NCBI]
|
0.00049878
|
|
|
VHL
|
[NCBI]
|
0.000454856
|
|
|
PDS
|
[NCBI]
|
0.000218053
|
|
|
arachnoid cysts, intracranial
|
[NCBI]
|
0.000163548
|
|
|
DFNA17
|
[NCBI]
|
0.000146787
|
|
|
aglossia-adactylia
|
[NCBI]
|
0.000141095
|
|
|
DFNA9
|
[NCBI]
|
0.000132315
|
|
|
canavan disease
|
[NCBI]
|
0.00012281
|
|
|
BOS1
|
[NCBI]
|
0.000120244
|
|
|
MTS
|
[NCBI]
|
0.000115724
|
|
|
NF2
|
[NCBI]
|
9.47407e-05
|
|
|
MAS
|
[NCBI]
|
7.16367e-05
|
|
|
CCD
|
[NCBI]
|
7.16367e-05
|
|
|
scribble, drosophila, homolog of
|
[NCBI]
|
4.86844e-05
|
|
|
VANGL2
|
[NCBI]
|
4.31798e-05
|
|
|
MYH9
|
[NCBI]
|
3.49638e-05
|
|
|
ASPA
|
[NCBI]
|
3.4101e-05
|
|
|
SLC26A4
|
[NCBI]
|
3.38351e-05
|
|
|
CHAT
|
[NCBI]
|
3.3499e-05
|
|
|
TNFRSF11B
|
[NCBI]
|
3.17062e-05
|
|
|
PCNA
|
[NCBI]
|
2.96707e-05
|
|
|
COL2A1
|
[NCBI]
|
2.90645e-05
|
|
|
mucopolysaccharidosis type ii
|
[NCBI]
|
2.67944e-05
|
|
|
GJB2
|
[NCBI]
|
2.44941e-05
|
|
|
NF1
|
[NCBI]
|
2.04556e-05
|
|
|
MUC1
|
[NCBI]
|
1.4185e-05
|
|
|
SLE
|
[NCBI]
|
1.08615e-05
|
|
|
CFTR
|
[NCBI]
|
6.16119e-06
|
|
|
CF
|
[NCBI]
|
4.62138e-06
|
|
|
MBP
|
[NCBI]
|
4.34477e-06
|
|
|
VEGF
|
[NCBI]
|
3.01224e-06
|
|
|
CCK
|
[NCBI]
|
2.65571e-06
|
|
|
TH
|
[NCBI]
|
1.56466e-06
|
|
|
RA
|
[NCBI]
|
5.9588e-07
|
|
|
EGF
|
[NCBI]
|
2.18583e-07
|
|
|
TNF
|
[NCBI]
|
2.29814e-08
|
|