|
OMIM |
Link |
Information gain |
01 |
|
spondyloepiphyseal dysplasia tarda, autosomal recessive
|
[NCBI]
|
0.00115589
|
|
|
ehlers-danlos syndrome, type vib
|
[NCBI]
|
0.000847142
|
|
|
spondylolisthesis
|
[NCBI]
|
0.000494879
|
|
|
spondylosis, cervical
|
[NCBI]
|
0.000137921
|
|
|
neural tube defects
|
[NCBI]
|
9.1078e-05
|
|
|
mannosidosis, alpha b, lysosomal
|
[NCBI]
|
8.58948e-05
|
|
|
MAN2B1
|
[NCBI]
|
7.48929e-05
|
|
|
aspartylglucosaminuria
|
[NCBI]
|
6.51968e-05
|
|
|
GFAP
|
[NCBI]
|
2.30904e-05
|
|