|
OMIM |
Link |
Information gain |
01 |
|
pseudohermaphroditism, female, with skeletal anomalies
|
[NCBI]
|
0.00163019
|
|
|
angioma, hereditary neurocutaneous
|
[NCBI]
|
0.00112601
|
|
|
lateral meningocele syndrome
|
[NCBI]
|
0.00106946
|
|
|
IS1
|
[NCBI]
|
0.00105127
|
|
|
lumbar stenosis, familial
|
[NCBI]
|
0.000442355
|
|
|
NSX
|
[NCBI]
|
0.000207178
|
|
|
OPLL
|
[NCBI]
|
0.000157537
|
|
|
RCDP1
|
[NCBI]
|
0.000120511
|
|
|
SCDO1
|
[NCBI]
|
0.000118776
|
|
|
ACH
|
[NCBI]
|
9.9077e-05
|
|
|
MFS
|
[NCBI]
|
8.02577e-05
|
|
|
lymphoma, non-hodgkin, familial
|
[NCBI]
|
6.41923e-05
|
|
|
ASL
|
[NCBI]
|
4.76917e-05
|
|
|
ASS
|
[NCBI]
|
4.27482e-05
|
|
|
GFAP
|
[NCBI]
|
1.58735e-05
|
|
|
EGF
|
[NCBI]
|
8.50919e-06
|
|