|
OMIM |
Link |
Information
gain |
01 |
|
|
immunoneurologic disorder, x-linked
|
[NCBI]
|
0.00138218
|
|
|
|
patent ductus arteriosus
|
[NCBI]
|
0.00101711
|
|
|
|
renal-hepatic-pancreatic dysplasia with dandy-walker cyst
|
[NCBI]
|
0.00101711
|
|
|
|
cerebral palsy, ataxic, autosomal recessive
|
[NCBI]
|
0.000904017
|
|
|
|
AMCN
|
[NCBI]
|
0.000761393
|
|
|
|
urogenital adysplasia, hereditary
|
[NCBI]
|
0.000512423
|
|
|
|
microcornea, glaucoma, and absent frontal sinuses
|
[NCBI]
|
0.000171939
|
|
|
|
hemoglobin, high oxygen saturation of
|
[NCBI]
|
0.000171939
|
|
|
|
TD1
|
[NCBI]
|
0.000168608
|
|
|
|
larsen-like syndrome, lethal type
|
[NCBI]
|
0.000144169
|
|
|
|
TD2
|
[NCBI]
|
0.000114445
|
|
|
|
cerebral palsy, spastic, symmetric, autosomal recessive
|
[NCBI]
|
0.000114445
|
|
|
|
omphalocele
|
[NCBI]
|
0.000111577
|
|
|
|
TSD
|
[NCBI]
|
4.78285e-05
|
|
|
|
CPI
|
[NCBI]
|
4.73166e-05
|
|
|
|
BWS
|
[NCBI]
|
4.04735e-05
|
|
|
|
NR3C2
|
[NCBI]
|
3.50524e-05
|
|
|
|
ALPL
|
[NCBI]
|
3.31254e-05
|
|
|
|
EPHX1
|
[NCBI]
|
3.24358e-05
|
|
|
|
L1CAM
|
[NCBI]
|
3.07475e-05
|
|
|
|
ACADM
|
[NCBI]
|
2.34738e-05
|
|
|
|
JAK2
|
[NCBI]
|
2.17006e-05
|
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
2.02918e-05
|
|
|
|
MG
|
[NCBI]
|
1.62877e-05
|
|
|
|
G6PD
|
[NCBI]
|
1.17001e-05
|
|
|
|
AFP
|
[NCBI]
|
8.43882e-06
|
|
|
|
APOE
|
[NCBI]
|
8.18778e-06
|
|
|
|
EPO
|
[NCBI]
|
6.80185e-06
|
|
|
|
SLE
|
[NCBI]
|
2.4888e-06
|
|
|
|
VEGF
|
[NCBI]
|
1.824e-06
|
|
