|
OMIM |
Link |
Information gain |
01 |
|
auditory neuropathy, x-linked, 1, with peripheral sensory neuropathy
|
[NCBI]
|
0.00145218
|
|
|
auditory neuropathy, autosomal dominant, 1
|
[NCBI]
|
0.00145218
|
|
|
HFM
|
[NCBI]
|
0.000761113
|
|
|
NF2
|
[NCBI]
|
0.000617688
|
|
|
optic atrophy, hearing loss, and peripheral neuropathy, autosomal recessive
|
[NCBI]
|
0.000194064
|
|
|
valproate embryopathy, susceptibility to
|
[NCBI]
|
0.000162475
|
|
|
deafness, aminoglycoside-induced
|
[NCBI]
|
0.000156777
|
|
|
DFNB9
|
[NCBI]
|
0.00015204
|
|
|
hypoparathyroidism, sensorineural deafness, and renal disease
|
[NCBI]
|
0.000144442
|
|
|
usher syndrome, type i
|
[NCBI]
|
0.000124035
|
|
|
CSA
|
[NCBI]
|
0.000104924
|
|
|
CMT1B
|
[NCBI]
|
0.000101125
|
|
|
fabry disease
|
[NCBI]
|
8.15972e-05
|
|
|
NGFB
|
[NCBI]
|
7.25529e-05
|
|
|
OTOF
|
[NCBI]
|
3.98141e-05
|
|
|
ACHE
|
[NCBI]
|
3.89151e-05
|
|
|
CHAT
|
[NCBI]
|
3.26756e-05
|
|
|
GDNF
|
[NCBI]
|
2.68775e-05
|
|
|
NGFR
|
[NCBI]
|
2.09625e-05
|
|
|
MAP2
|
[NCBI]
|
1.69029e-05
|
|
|
MBP
|
[NCBI]
|
1.65442e-05
|
|
|
BDNF
|
[NCBI]
|
1.31097e-05
|
|
|
GFAP
|
[NCBI]
|
1.09305e-05
|
|
|
CNTF
|
[NCBI]
|
1.04645e-05
|
|
|
SPP1
|
[NCBI]
|
9.49258e-06
|
|
|
G6PD
|
[NCBI]
|
9.18769e-06
|
|
|
PCNA
|
[NCBI]
|
3.06311e-06
|
|
|
CF
|
[NCBI]
|
1.53266e-08
|
|