|
OMIM |
Link |
Information gain |
01 |
|
corneal hypesthesia, familial
|
[NCBI]
|
0.00107364
|
|
|
indifference to pain, congenital, autosomal dominant
|
[NCBI]
|
0.000938013
|
|
|
IH
|
[NCBI]
|
0.000750767
|
|
|
HSAN2
|
[NCBI]
|
0.000190029
|
|
|
hypertrophic neuropathy and cataract
|
[NCBI]
|
0.000145155
|
|
|
insensitivity to pain with hyperplastic myelinopathy
|
[NCBI]
|
0.000145155
|
|
|
cyprus facial neuromusculoskeletal syndrome
|
[NCBI]
|
0.000145155
|
|
|
adie pupil
|
[NCBI]
|
0.000108698
|
|
|
neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive
|
[NCBI]
|
0.000108698
|
|
|
charcot-marie-tooth disease, axonal, type 2j
|
[NCBI]
|
0.000101342
|
|
|
indifference to pain, congenital, autosomal recessive
|
[NCBI]
|
8.67829e-05
|
|
|
CIPA
|
[NCBI]
|
8.0832e-05
|
|
|
lymphedema-distichiasis syndrome
|
[NCBI]
|
7.92529e-05
|
|
|
HNA
|
[NCBI]
|
7.78148e-05
|
|
|
NGFB
|
[NCBI]
|
7.18305e-05
|
|
|
tyrosinemia, type i
|
[NCBI]
|
4.64948e-05
|
|
|
MPZ
|
[NCBI]
|
4.36643e-05
|
|
|
AKR1B1
|
[NCBI]
|
3.79048e-05
|
|
|
PWS
|
[NCBI]
|
2.45514e-05
|
|
|
VIP
|
[NCBI]
|
2.04899e-05
|
|
|
NPY
|
[NCBI]
|
1.58525e-05
|
|
|
VEGF
|
[NCBI]
|
3.04201e-06
|
|
|
SLE
|
[NCBI]
|
1.38534e-06
|
|