|
OMIM |
Link |
Information
gain |
01 |
|
|
tune deafness
|
[NCBI]
|
0.00110387
|
|
|
|
auditory neuropathy, autosomal dominant, 1
|
[NCBI]
|
0.00110387
|
|
|
|
auditory neuropathy, x-linked, 1, with peripheral sensory neuropathy
|
[NCBI]
|
0.00110387
|
|
|
|
mohr syndrome
|
[NCBI]
|
0.000869022
|
|
|
|
varadi-papp syndrome
|
[NCBI]
|
0.000847798
|
|
|
|
JBTS1
|
[NCBI]
|
0.000710915
|
|
|
|
alport syndrome, autosomal dominant
|
[NCBI]
|
0.000701422
|
|
|
|
musical perfect pitch
|
[NCBI]
|
0.000198192
|
|
|
|
wildervanck syndrome
|
[NCBI]
|
0.000120396
|
|
|
|
DFNA20
|
[NCBI]
|
0.000116365
|
|
|
|
USH1D
|
[NCBI]
|
0.000105413
|
|
|
|
indifference to pain, congenital, autosomal recessive
|
[NCBI]
|
9.99223e-05
|
|
|
|
DYX2
|
[NCBI]
|
9.43734e-05
|
|
|
|
DYX1
|
[NCBI]
|
8.56852e-05
|
|
|
|
LKS
|
[NCBI]
|
7.69714e-05
|
|
|
|
CMT1B
|
[NCBI]
|
7.37298e-05
|
|
|
|
PAX6
|
[NCBI]
|
6.18627e-05
|
|
|
|
ADHD
|
[NCBI]
|
5.88942e-05
|
|
|
|
SCZD
|
[NCBI]
|
5.84993e-05
|
|
|
|
PMD
|
[NCBI]
|
5.29393e-05
|
|
|
|
BSN
|
[NCBI]
|
4.22001e-05
|
|
|
|
CHRNA7
|
[NCBI]
|
3.89443e-05
|
|
|
|
AT
|
[NCBI]
|
3.73996e-05
|
|
|
|
ACTG1
|
[NCBI]
|
3.68536e-05
|
|
|
|
HSR
|
[NCBI]
|
3.33104e-05
|
|
|
|
CDH23
|
[NCBI]
|
3.33104e-05
|
|
|
|
TS
|
[NCBI]
|
3.11627e-05
|
|
|
|
BDNF
|
[NCBI]
|
1.95742e-05
|
|
|
|
AR
|
[NCBI]
|
6.42093e-06
|
|
|
|
CCK
|
[NCBI]
|
5.66627e-06
|
|
|
|
EPO
|
[NCBI]
|
5.5338e-06
|
|
|
|
AVP
|
[NCBI]
|
4.99082e-06
|
|
|
|
NPY
|
[NCBI]
|
3.97909e-06
|
|
