|
OMIM |
Link |
Information gain |
01 |
|
osteogenesis imperfecta, type v
|
[NCBI]
|
0.00244453
|
|
|
osteogenesis imperfecta, type vi
|
[NCBI]
|
0.00244453
|
|
|
PTH
|
[NCBI]
|
0.000563241
|
|
|
TNFRSF11B
|
[NCBI]
|
0.000247728
|
|
|
osteogenesis imperfecta, type i
|
[NCBI]
|
0.000159998
|
|
|
osteolysis, hereditary multicentric
|
[NCBI]
|
0.000138528
|
|
|
MONA
|
[NCBI]
|
0.000130792
|
|
|
winchester syndrome
|
[NCBI]
|
0.000120461
|
|
|
OPPG
|
[NCBI]
|
0.000113393
|
|
|
PDP
|
[NCBI]
|
0.000110545
|
|
|
osteogenesis imperfecta, type iv
|
[NCBI]
|
9.54804e-05
|
|
|
osteogenesis imperfecta, type iii
|
[NCBI]
|
9.28876e-05
|
|
|
VDR
|
[NCBI]
|
8.35645e-05
|
|
|
RA
|
[NCBI]
|
7.32929e-05
|
|
|
JMML
|
[NCBI]
|
6.58357e-05
|
|
|
MAS
|
[NCBI]
|
5.60641e-05
|
|
|
temporal arteritis
|
[NCBI]
|
3.11582e-05
|
|
|
ACP5
|
[NCBI]
|
2.85321e-05
|
|
|
ADORA3
|
[NCBI]
|
1.85178e-05
|
|
|
PD
|
[NCBI]
|
1.83103e-05
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
1.16079e-05
|
|
|
BGLAP
|
[NCBI]
|
9.98594e-06
|
|
|
COMP
|
[NCBI]
|
8.51067e-06
|
|
|
PDCD8
|
[NCBI]
|
8.0498e-06
|
|
|
NR1I2
|
[NCBI]
|
7.50662e-06
|
|
|
EGF
|
[NCBI]
|
7.38551e-06
|
|
|
TNF
|
[NCBI]
|
7.23682e-06
|
|
|
HDC
|
[NCBI]
|
7.02389e-06
|
|
|
SLE
|
[NCBI]
|
4.25706e-06
|
|
|
KLK3
|
[NCBI]
|
4.18288e-06
|
|
|
ALB
|
[NCBI]
|
4.17691e-06
|
|
|
CF
|
[NCBI]
|
4.04109e-06
|
|
|
PTHLH
|
[NCBI]
|
3.35048e-06
|
|
|
SPP1
|
[NCBI]
|
2.40648e-06
|
|
|
SHBG
|
[NCBI]
|
2.24346e-06
|
|
|
CAT
|
[NCBI]
|
2.5396e-07
|
|
|
VEGF
|
[NCBI]
|
1.18996e-07
|
|
|
PCNA
|
[NCBI]
|
1.07933e-07
|
|
|
MPO
|
[NCBI]
|
2.2152e-09
|
|