|
OMIM |
Link |
Information gain |
01 |
|
ehlers-danlos syndrome, type vii, autosomal recessive
|
[NCBI]
|
0.0008869
|
|
|
ehlers-danlos syndrome, type vii, autosomal dominant
|
[NCBI]
|
0.000299241
|
|
|
osteogenesis imperfecta, type iia
|
[NCBI]
|
0.000107969
|
|
|
ADAMTS14
|
[NCBI]
|
9.54362e-05
|
|
|
ADAMTS4
|
[NCBI]
|
8.76425e-05
|
|
|
COL1A1
|
[NCBI]
|
5.14946e-05
|
|
|
ADAMTS2
|
[NCBI]
|
4.52161e-05
|
|
|
ADAMTS5
|
[NCBI]
|
4.05951e-05
|
|
|
ADAMTS1
|
[NCBI]
|
3.81643e-05
|
|
|
COL1A2
|
[NCBI]
|
2.32428e-05
|
|
|
PTGS2
|
[NCBI]
|
2.22665e-05
|
|
|
JAK2
|
[NCBI]
|
1.83794e-05
|
|
|
COMP
|
[NCBI]
|
1.77133e-05
|
|
|
OSM
|
[NCBI]
|
1.53052e-05
|
|
|
TNF
|
[NCBI]
|
5.5348e-06
|
|
|
RA
|
[NCBI]
|
6.94076e-07
|
|