|
OMIM |
Link |
Information gain |
01 |
|
ATD1
|
[NCBI]
|
0.00394655
|
|
|
spondylometaphyseal dysplasia, kozlowski type
|
[NCBI]
|
0.00232265
|
|
|
bone size quantitative trait locus 3
|
[NCBI]
|
0.00136729
|
|
|
upington disease
|
[NCBI]
|
0.00136729
|
|
|
microcephalic osteodysplastic primordial dwarfism, type iii
|
[NCBI]
|
0.000939888
|
|
|
bone size quantitative trait locus 1
|
[NCBI]
|
0.000939888
|
|
|
spondyloepiphyseal dysplasia tarda, autosomal dominant
|
[NCBI]
|
0.000939888
|
|
|
microcephalic osteodysplastic primordial dwarfism, type i
|
[NCBI]
|
0.000807956
|
|
|
ulna and fibula, absence of, with severe limb deficiency
|
[NCBI]
|
0.000751854
|
|
|
BMND3
|
[NCBI]
|
0.000726199
|
|
|
hypertension with brachydactyly
|
[NCBI]
|
0.000694531
|
|
|
proteus syndrome
|
[NCBI]
|
0.000475184
|
|
|
SPS
|
[NCBI]
|
0.000460573
|
|
|
klippel-trenaunay-weber syndrome
|
[NCBI]
|
0.000359351
|
|
|
HCH
|
[NCBI]
|
0.000339304
|
|
|
osteomesopyknosis
|
[NCBI]
|
0.000330968
|
|
|
spondyloepimetaphyseal dysplasia, strudwick type
|
[NCBI]
|
0.000243512
|
|
|
CCD
|
[NCBI]
|
0.000234475
|
|
|
FFS
|
[NCBI]
|
0.000232164
|
|
|
sao paulo mca/mr syndrome
|
[NCBI]
|
0.000192271
|
|
|
eiken skeletal dysplasia
|
[NCBI]
|
0.000192271
|
|
|
acrodysplasia with ossification abnormalities, short stature, and fibular hypoplasia
|
[NCBI]
|
0.000153026
|
|
|
aneurysmal bone cysts
|
[NCBI]
|
0.000153026
|
|
|
hyaluronidase deficiency
|
[NCBI]
|
0.000153026
|
|
|
pelvic hypoplasia with lower-limb arthrogryposis
|
[NCBI]
|
0.000153026
|
|
|
thoracopelvic dysostosis
|
[NCBI]
|
0.000153026
|
|
|
hyaluronan metabolism, defect in
|
[NCBI]
|
0.000153026
|
|
|
ulna metaphyseal dysplasia syndrome
|
[NCBI]
|
0.000153026
|
|
|
ankylosing vertebral hyperostosis with tylosis
|
[NCBI]
|
0.000138233
|
|
|
OPTA1
|
[NCBI]
|
0.000138233
|
|
|
gurrieri syndrome
|
[NCBI]
|
0.000138233
|
|
|
ACH
|
[NCBI]
|
0.000131453
|
|
|
TLPD
|
[NCBI]
|
0.000128637
|
|
|
growth-mental deficiency syndrome of myhre
|
[NCBI]
|
0.000115837
|
|
|
avascular necrosis of femoral head, primary
|
[NCBI]
|
0.000115837
|
|
|
fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly
|
[NCBI]
|
0.000115837
|
|
|
OSMED
|
[NCBI]
|
0.000115837
|
|
|
MCDS
|
[NCBI]
|
0.000115837
|
|
|
pituitary dwarfism i
|
[NCBI]
|
0.000115837
|
|
|
hyperostosis corticalis generalisata, benign form of worth, with torus palatinus
|
[NCBI]
|
0.000111124
|
|
|
OPTA2
|
[NCBI]
|
0.000111124
|
|
|
pycnodysostosis
|
[NCBI]
|
0.000103575
|
|
|
alkaptonuria
|
[NCBI]
|
0.000100453
|
|
|
paget disease, juvenile
|
[NCBI]
|
9.50988e-05
|
|
|
FMD
|
[NCBI]
|
9.0617e-05
|
|
|
camurati-engelmann disease
|
[NCBI]
|
8.86232e-05
|
|
|
PTH
|
[NCBI]
|
8.51463e-05
|
|
|
SLSN1
|
[NCBI]
|
8.50245e-05
|
|
|
mucolipidosis iiia
|
[NCBI]
|
8.33887e-05
|
|
|
HFTC
|
[NCBI]
|
8.03855e-05
|
|
|
PPS
|
[NCBI]
|
7.9e-05
|
|
|
hypophosphatasia, infantile
|
[NCBI]
|
7.9e-05
|
|
|
mucopolysaccharidosis type vi
|
[NCBI]
|
7.7682e-05
|
|
|
mucopolysaccharidosis type vii
|
[NCBI]
|
7.64255e-05
|
|
|
CFNS
|
[NCBI]
|
7.5225e-05
|
|
|
EVC
|
[NCBI]
|
7.2974e-05
|
|
|
BMD
|
[NCBI]
|
6.63232e-05
|
|
|
HYAL1
|
[NCBI]
|
5.41316e-05
|
|
|
PSACH
|
[NCBI]
|
5.33702e-05
|
|
|
TBX4
|
[NCBI]
|
4.96571e-05
|
|
|
COL10A1
|
[NCBI]
|
4.38763e-05
|
|
|
PTHR1
|
[NCBI]
|
3.95374e-05
|
|
|
SLE
|
[NCBI]
|
3.67128e-05
|
|
|
GUSB
|
[NCBI]
|
3.03319e-05
|
|
|
FMF
|
[NCBI]
|
2.08962e-05
|
|
|
VDR
|
[NCBI]
|
1.45069e-05
|
|
|
KLK3
|
[NCBI]
|
1.09268e-05
|
|