|
OMIM |
Link |
Information gain |
01 |
|
corneal dystrophy, crystalline, of schnyder
|
[NCBI]
|
0.00188183
|
|
|
PPS
|
[NCBI]
|
0.00148125
|
|
|
arthrogryposis-like disorder
|
[NCBI]
|
0.00146221
|
|
|
hip dysplasia, beukes type
|
[NCBI]
|
0.00146221
|
|
|
OD
|
[NCBI]
|
0.00145146
|
|
|
trichoscyphodysplasia
|
[NCBI]
|
0.00115153
|
|
|
metaphyseal acroscyphodysplasia
|
[NCBI]
|
0.00115153
|
|
|
DBQD
|
[NCBI]
|
0.000735764
|
|
|
behcet syndrome
|
[NCBI]
|
0.00061405
|
|
|
pena-shokeir syndrome, type i
|
[NCBI]
|
0.000495203
|
|
|
genu valgum, st. helena familial
|
[NCBI]
|
0.000375039
|
|
|
LRS1
|
[NCBI]
|
0.000339254
|
|
|
CCAL2
|
[NCBI]
|
0.000333961
|
|
|
osteoarthritis
|
[NCBI]
|
0.00021732
|
|
|
hypophosphatasia, infantile
|
[NCBI]
|
0.000188631
|
|
|
ulna metaphyseal dysplasia syndrome
|
[NCBI]
|
0.000148072
|
|
|
carpenter syndrome
|
[NCBI]
|
0.000133285
|
|
|
EDM2
|
[NCBI]
|
0.000133285
|
|
|
ankylosing vertebral hyperostosis with tylosis
|
[NCBI]
|
0.000133285
|
|
|
osteochondrosis deformans tibiae, familial infantile type
|
[NCBI]
|
0.000133285
|
|
|
hunter-mcalpine craniosynostosis syndrome
|
[NCBI]
|
0.000116575
|
|
|
ruvalcaba syndrome
|
[NCBI]
|
0.000110908
|
|
|
noonan-like/multiple giant cell lesion syndrome
|
[NCBI]
|
0.000106201
|
|
|
fibromatosis, juvenile hyaline
|
[NCBI]
|
0.000102178
|
|
|
osseous heteroplasia, progressive
|
[NCBI]
|
0.000102178
|
|
|
ANKH
|
[NCBI]
|
0.000100704
|
|
|
RA
|
[NCBI]
|
0.000100143
|
|
|
SEDT
|
[NCBI]
|
9.55481e-05
|
|
|
EDM1
|
[NCBI]
|
9.02066e-05
|
|
|
WGN1
|
[NCBI]
|
9.02066e-05
|
|
|
COFS1
|
[NCBI]
|
8.57369e-05
|
|
|
CACP
|
[NCBI]
|
8.37493e-05
|
|
|
CMDD
|
[NCBI]
|
8.01629e-05
|
|
|
STL1
|
[NCBI]
|
7.69962e-05
|
|
|
FMF
|
[NCBI]
|
6.66169e-05
|
|
|
RTS
|
[NCBI]
|
6.07389e-05
|
|
|
AMC
|
[NCBI]
|
5.56275e-05
|
|
|
VWS
|
[NCBI]
|
5.43375e-05
|
|
|
NPS
|
[NCBI]
|
5.37164e-05
|
|
|
MB
|
[NCBI]
|
5.33809e-05
|
|
|
SDS
|
[NCBI]
|
4.9754e-05
|
|
|
ASPN
|
[NCBI]
|
4.92882e-05
|
|
|
COL9A2
|
[NCBI]
|
4.78387e-05
|
|
|
ACH
|
[NCBI]
|
4.21774e-05
|
|
|
contractural arachnodactyly, congenital
|
[NCBI]
|
3.87232e-05
|
|
|
CNTF
|
[NCBI]
|
3.58619e-05
|
|
|
COL2A1
|
[NCBI]
|
3.14748e-05
|
|
|
DFSP
|
[NCBI]
|
3.07362e-05
|
|
|
SLE
|
[NCBI]
|
2.85314e-05
|
|
|
ALK
|
[NCBI]
|
2.35842e-05
|
|
|
NF1
|
[NCBI]
|
2.28342e-05
|
|
|
PF4
|
[NCBI]
|
1.806e-05
|
|
|
CVID
|
[NCBI]
|
1.59731e-05
|
|
|
VDR
|
[NCBI]
|
1.16761e-05
|
|
|
CEACAM5
|
[NCBI]
|
6.97114e-06
|
|
|
PCNA
|
[NCBI]
|
5.0143e-06
|
|
|
PTH
|
[NCBI]
|
3.0975e-06
|
|
|
PD
|
[NCBI]
|
2.73066e-06
|
|
|
NPY
|
[NCBI]
|
2.50024e-06
|
|