|
OMIM |
Link |
Information gain |
01 |
|
IS1
|
[NCBI]
|
0.0224514
|
|
|
BMND3
|
[NCBI]
|
0.00134656
|
|
|
PTH
|
[NCBI]
|
0.00119668
|
|
|
vertebral hypoplasia with lumbar kyphosis
|
[NCBI]
|
0.00113682
|
|
|
IDD
|
[NCBI]
|
0.000836823
|
|
|
osteogenesis imperfecta, type vi
|
[NCBI]
|
0.000827228
|
|
|
VDR
|
[NCBI]
|
0.00081128
|
|
|
torus palatinus and torus mandibularis
|
[NCBI]
|
0.000636418
|
|
|
spondyloepimetaphyseal dysplasia with multiple dislocations
|
[NCBI]
|
0.000636418
|
|
|
costovertebral segmentation anomalies
|
[NCBI]
|
0.000636418
|
|
|
opsismodysplasia
|
[NCBI]
|
0.000581136
|
|
|
spondyloepimetaphyseal dysplasia, sponastrime type
|
[NCBI]
|
0.000537366
|
|
|
CARASIL
|
[NCBI]
|
0.000501203
|
|
|
spondyloenchondrodysplasia
|
[NCBI]
|
0.000501203
|
|
|
RA
|
[NCBI]
|
0.000451776
|
|
|
spondylolisthesis
|
[NCBI]
|
0.000280093
|
|
|
SEDT
|
[NCBI]
|
0.000192961
|
|
|
osteoporosis
|
[NCBI]
|
0.000192961
|
|
|
TNFRSF11B
|
[NCBI]
|
0.000188956
|
|
|
neural tube defects
|
[NCBI]
|
0.000187046
|
|
|
CD
|
[NCBI]
|
0.00016855
|
|
|
BGLAP
|
[NCBI]
|
0.000139958
|
|
|
NSX
|
[NCBI]
|
0.000127759
|
|
|
spondylosis, cervical
|
[NCBI]
|
0.000127759
|
|
|
SCDO1
|
[NCBI]
|
0.000121088
|
|
|
ankylosing vertebral hyperostosis with tylosis
|
[NCBI]
|
0.000113012
|
|
|
OPTA1
|
[NCBI]
|
0.000113012
|
|
|
lumbar stenosis, familial
|
[NCBI]
|
0.000113012
|
|
|
native american myopathy
|
[NCBI]
|
0.000103463
|
|
|
caudal duplication anomaly
|
[NCBI]
|
0.000103463
|
|
|
HCA2
|
[NCBI]
|
9.63817e-05
|
|
|
GCS1
|
[NCBI]
|
9.63817e-05
|
|
|
d-2-@hydroxyglutaric aciduria
|
[NCBI]
|
9.63817e-05
|
|
|
ACP5
|
[NCBI]
|
8.66384e-05
|
|
|
OPTA2
|
[NCBI]
|
8.60886e-05
|
|
|
BMND1
|
[NCBI]
|
8.60886e-05
|
|
|
ACH
|
[NCBI]
|
8.35877e-05
|
|
|
OGD
|
[NCBI]
|
8.21052e-05
|
|
|
osteogenesis imperfecta, type iii
|
[NCBI]
|
6.80089e-05
|
|
|
osteogenesis imperfecta, type iv
|
[NCBI]
|
6.80089e-05
|
|
|
gm1-gangliosidosis, type ii
|
[NCBI]
|
6.80089e-05
|
|
|
weaver syndrome
|
[NCBI]
|
6.59053e-05
|
|
|
currarino syndrome
|
[NCBI]
|
6.59053e-05
|
|
|
chondrodysplasia punctata, autosomal dominant
|
[NCBI]
|
6.39579e-05
|
|
|
SCN1
|
[NCBI]
|
6.39579e-05
|
|
|
sacral defect with anterior meningocele
|
[NCBI]
|
6.04517e-05
|
|
|
growth hormone insensitivity syndrome
|
[NCBI]
|
5.88622e-05
|
|
|
AIS
|
[NCBI]
|
5.75367e-05
|
|
|
gm1-gangliosidosis, type iii
|
[NCBI]
|
5.73654e-05
|
|
|
CILP
|
[NCBI]
|
5.64981e-05
|
|
|
MNS
|
[NCBI]
|
5.59515e-05
|
|
|
SEDC
|
[NCBI]
|
5.59515e-05
|
|
|
MFS
|
[NCBI]
|
5.0205e-05
|
|
|
SLE
|
[NCBI]
|
4.91574e-05
|
|
|
RSMD1
|
[NCBI]
|
4.78059e-05
|
|
|
SHBG
|
[NCBI]
|
4.73768e-05
|
|
|
mannosidosis, alpha b, lysosomal
|
[NCBI]
|
4.02236e-05
|
|
|
CRMO
|
[NCBI]
|
3.75106e-05
|
|
|
APS1
|
[NCBI]
|
3.39723e-05
|
|
|
VEGF
|
[NCBI]
|
3.38661e-05
|
|
|
CDX1
|
[NCBI]
|
3.21105e-05
|
|
|
PLXNA2
|
[NCBI]
|
3.21105e-05
|
|
|
CLS
|
[NCBI]
|
3.18972e-05
|
|
|
neuraminidase deficiency
|
[NCBI]
|
3.14086e-05
|
|
|
TD1
|
[NCBI]
|
3.09311e-05
|
|
|
PSACH
|
[NCBI]
|
3.04643e-05
|
|
|
AGC1
|
[NCBI]
|
2.88584e-05
|
|
|
COL9A3
|
[NCBI]
|
2.88584e-05
|
|
|
osteogenesis imperfecta, type i
|
[NCBI]
|
2.86962e-05
|
|
|
AXIN1
|
[NCBI]
|
2.76613e-05
|
|
|
SEMA7A
|
[NCBI]
|
2.66377e-05
|
|
|
CASR
|
[NCBI]
|
2.59286e-05
|
|
|
HOXA10
|
[NCBI]
|
2.4951e-05
|
|
|
TRAPPC2
|
[NCBI]
|
2.42384e-05
|
|
|
COL11A1
|
[NCBI]
|
2.42384e-05
|
|
|
SLC30A3
|
[NCBI]
|
2.42384e-05
|
|
|
PRPH
|
[NCBI]
|
2.35916e-05
|
|
|
ADIPOR1
|
[NCBI]
|
2.35916e-05
|
|
|
GHRHR
|
[NCBI]
|
2.24539e-05
|
|
|
MDD
|
[NCBI]
|
2.21684e-05
|
|
|
MAN2B1
|
[NCBI]
|
2.0228e-05
|
|
|
BCNS
|
[NCBI]
|
1.94791e-05
|
|
|
NF1
|
[NCBI]
|
1.9023e-05
|
|
|
DIABLO
|
[NCBI]
|
1.88533e-05
|
|
|
CTSK
|
[NCBI]
|
1.85489e-05
|
|
|
adenylyl cyclase, soluble
|
[NCBI]
|
1.79782e-05
|
|
|
TNFRSF1B
|
[NCBI]
|
1.67327e-05
|
|
|
PMD
|
[NCBI]
|
1.64405e-05
|
|
|
BDNF
|
[NCBI]
|
1.59836e-05
|
|
|
TACR1
|
[NCBI]
|
1.53063e-05
|
|
|
SMS
|
[NCBI]
|
1.52174e-05
|
|
|
GH1
|
[NCBI]
|
1.46117e-05
|
|
|
SMAX1
|
[NCBI]
|
1.44558e-05
|
|
|
neuraminidase deficiency with beta-galactosidase deficiency
|
[NCBI]
|
1.4449e-05
|
|
|
ACHE
|
[NCBI]
|
1.35056e-05
|
|
|
ATF3
|
[NCBI]
|
1.22888e-05
|
|
|
COL1A1
|
[NCBI]
|
1.22888e-05
|
|
|
AR
|
[NCBI]
|
1.20918e-05
|
|
|
ESR1
|
[NCBI]
|
1.18478e-05
|
|
|
AVP
|
[NCBI]
|
1.09249e-05
|
|
|
BMP2
|
[NCBI]
|
1.07772e-05
|
|
|
VIP
|
[NCBI]
|
1.07522e-05
|
|
|
LCT
|
[NCBI]
|
1.04308e-05
|
|
|
CRH
|
[NCBI]
|
1.00995e-05
|
|
|
PPARG
|
[NCBI]
|
1.00247e-05
|
|
|
TRPV1
|
[NCBI]
|
9.86978e-06
|
|
|
TNF
|
[NCBI]
|
8.96458e-06
|
|
|
LEP
|
[NCBI]
|
8.28096e-06
|
|
|
FGFR1
|
[NCBI]
|
8.16706e-06
|
|
|
TNFSF11
|
[NCBI]
|
7.78643e-06
|
|
|
CF
|
[NCBI]
|
7.38099e-06
|
|
|
GDNF
|
[NCBI]
|
7.01723e-06
|
|
|
NGFB
|
[NCBI]
|
6.52542e-06
|
|
|
SLC18A3
|
[NCBI]
|
4.77991e-06
|
|
|
COMP
|
[NCBI]
|
4.53679e-06
|
|
|
FMF
|
[NCBI]
|
4.53061e-06
|
|
|
NPY
|
[NCBI]
|
4.31673e-06
|
|
|
TH
|
[NCBI]
|
3.44666e-06
|
|
|
temporal arteritis
|
[NCBI]
|
3.04603e-06
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
2.30674e-06
|
|
|
lymphoma, non-hodgkin, familial
|
[NCBI]
|
2.1724e-06
|
|
|
KLK3
|
[NCBI]
|
2.05762e-06
|
|
|
GFAP
|
[NCBI]
|
1.31607e-06
|
|
|
MPO
|
[NCBI]
|
1.30983e-06
|
|
|
AFP
|
[NCBI]
|
1.14353e-06
|
|
|
PRL
|
[NCBI]
|
1.10576e-06
|
|
|
GAL
|
[NCBI]
|
1.0904e-06
|
|
|
TLR4
|
[NCBI]
|
8.05238e-07
|
|
|
CHAT
|
[NCBI]
|
6.48009e-07
|
|
|
APOE
|
[NCBI]
|
6.13327e-07
|
|
|
PTHLH
|
[NCBI]
|
3.69634e-07
|
|
|
TNFSF6
|
[NCBI]
|
3.09892e-07
|
|
|
CEACAM5
|
[NCBI]
|
1.54876e-07
|
|
|
ADCYAP1
|
[NCBI]
|
1.02268e-07
|
|
|
CNTF
|
[NCBI]
|
3.03711e-08
|
|