|
OMIM |
Link |
Information
gain |
01 |
|
|
EOCA
|
[NCBI]
|
0.00805154
|
|
|
|
DA10
|
[NCBI]
|
0.00127744
|
|
|
|
CMT2B2
|
[NCBI]
|
0.000847798
|
|
|
|
hereditary motor and sensory neuropathy v
|
[NCBI]
|
0.000761393
|
|
|
|
amyotrophy, monomelic
|
[NCBI]
|
0.000729587
|
|
|
|
FRDA
|
[NCBI]
|
0.000502569
|
|
|
|
dystonia with ringbinden
|
[NCBI]
|
0.000158423
|
|
|
|
cortical dysplasia-focal epilepsy syndrome
|
[NCBI]
|
0.000158423
|
|
|
|
amenorrhea-galactorrhea syndrome
|
[NCBI]
|
0.000130657
|
|
|
|
GRTH
|
[NCBI]
|
0.000104299
|
|
|
|
thyrotropin deficiency, isolated
|
[NCBI]
|
0.000104299
|
|
|
|
INAD1
|
[NCBI]
|
9.55827e-05
|
|
|
|
LGMD1A
|
[NCBI]
|
9.13596e-05
|
|
|
|
HMN5
|
[NCBI]
|
8.63434e-05
|
|
|
|
cerebrotendinous xanthomatosis
|
[NCBI]
|
8.63434e-05
|
|
|
|
HNA
|
[NCBI]
|
8.00649e-05
|
|
|
|
niemann-pick disease, type a
|
[NCBI]
|
7.61714e-05
|
|
|
|
TGD
|
[NCBI]
|
7.61714e-05
|
|
|
|
RMD
|
[NCBI]
|
7.53072e-05
|
|
|
|
HYPP
|
[NCBI]
|
6.60447e-05
|
|
|
|
RSTS
|
[NCBI]
|
6.45244e-05
|
|
|
|
AMC
|
[NCBI]
|
6.0569e-05
|
|
|
|
ALS1
|
[NCBI]
|
5.44854e-05
|
|
|
|
SCA2
|
[NCBI]
|
5.33609e-05
|
|
|
|
CNTNAP2
|
[NCBI]
|
5.02492e-05
|
|
|
|
SCA1
|
[NCBI]
|
4.79397e-05
|
|
|
|
L1CAM
|
[NCBI]
|
3.45946e-05
|
|
|
|
FXN
|
[NCBI]
|
3.39014e-05
|
|
|
|
THRB
|
[NCBI]
|
3.20441e-05
|
|
|
|
FRAP1
|
[NCBI]
|
1.85667e-05
|
|
|
|
RA
|
[NCBI]
|
1.35368e-05
|
|
|
|
AFP
|
[NCBI]
|
1.20134e-05
|
|
|
|
MG
|
[NCBI]
|
6.61328e-06
|
|
