|
OMIM |
Link |
Information gain |
01 |
|
tibia, hypoplasia of, with polydactyly
|
[NCBI]
|
0.0084004
|
|
|
SHFLD1
|
[NCBI]
|
0.00669214
|
|
|
femur, unilateral bifid, with monodactylous ectrodactyly
|
[NCBI]
|
0.00529225
|
|
|
PTH
|
[NCBI]
|
0.00130878
|
|
|
tibial torsion, bilateral medial
|
[NCBI]
|
0.00116638
|
|
|
mesomelic dwarfism of hypoplastic tibia and radius type
|
[NCBI]
|
0.00116638
|
|
|
caffey disease
|
[NCBI]
|
0.0010529
|
|
|
OD
|
[NCBI]
|
0.000859483
|
|
|
clubbing of digits
|
[NCBI]
|
0.000856615
|
|
|
nievergelt syndrome
|
[NCBI]
|
0.000856615
|
|
|
tibial hemimelia
|
[NCBI]
|
0.000800197
|
|
|
brachyphalangy, polydactyly, and tibial aplasia/hypoplasia
|
[NCBI]
|
0.000700843
|
|
|
acromelic frontonasal dysostosis
|
[NCBI]
|
0.00056605
|
|
|
GO
|
[NCBI]
|
0.000529712
|
|
|
BMND3
|
[NCBI]
|
0.000529712
|
|
|
OFD4
|
[NCBI]
|
0.000529712
|
|
|
osteochondrosis deformans tibiae, familial infantile type
|
[NCBI]
|
0.000525227
|
|
|
short rib-polydactyly syndrome, type iv
|
[NCBI]
|
0.00049878
|
|
|
kyphomelic dysplasia
|
[NCBI]
|
0.00047189
|
|
|
fibular aplasia, tibial campomelia, and oligosyndactyly syndrome
|
[NCBI]
|
0.000461555
|
|
|
mohr syndrome
|
[NCBI]
|
0.000448139
|
|
|
SPP1
|
[NCBI]
|
0.000441379
|
|
|
OSCS
|
[NCBI]
|
0.000407698
|
|
|
bowing of legs, anterior, with dwarfism
|
[NCBI]
|
0.000407569
|
|
|
ACP5
|
[NCBI]
|
0.000359309
|
|
|
tibia vara
|
[NCBI]
|
0.000349883
|
|
|
osteofibrous dysplasia
|
[NCBI]
|
0.000349883
|
|
|
tibia, absence of, with polydactyly
|
[NCBI]
|
0.000349883
|
|
|
tibial muscular dystrophy, tardive
|
[NCBI]
|
0.000313257
|
|
|
camurati-engelmann disease
|
[NCBI]
|
0.000313257
|
|
|
HHS
|
[NCBI]
|
0.000295839
|
|
|
TNFRSF11B
|
[NCBI]
|
0.000243961
|
|
|
thrombocytopenia-absent radius syndrome
|
[NCBI]
|
0.000231705
|
|
|
campomelic dysplasia
|
[NCBI]
|
0.000227657
|
|
|
HEPOD
|
[NCBI]
|
0.00020264
|
|
|
IS1
|
[NCBI]
|
0.000201478
|
|
|
SLE
|
[NCBI]
|
0.000183234
|
|
|
tibia, absence or hypoplasia of, with polydactyly, retrocerebellar arachnoid cyst, and other anomalies
|
[NCBI]
|
0.000174808
|
|
|
syndactyly, type iv
|
[NCBI]
|
0.000174808
|
|
|
osteosclerosis with ichthyosis and fractures
|
[NCBI]
|
0.000174808
|
|
|
mesomelic dysplasia, savarirayan type
|
[NCBI]
|
0.000174808
|
|
|
dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, and mental retardation
|
[NCBI]
|
0.000174808
|
|
|
ulna and fibula, hypoplasia of
|
[NCBI]
|
0.000174808
|
|
|
paget disease, extramammary
|
[NCBI]
|
0.000174808
|
|
|
adamantinoma of long bones
|
[NCBI]
|
0.000174808
|
|
|
ribbing disease
|
[NCBI]
|
0.000174808
|
|
|
genochondromatosis
|
[NCBI]
|
0.000174808
|
|
|
osteoid osteoma
|
[NCBI]
|
0.000174808
|
|
|
LWD
|
[NCBI]
|
0.000141473
|
|
|
RTS
|
[NCBI]
|
0.000136246
|
|
|
BGLAP
|
[NCBI]
|
0.000136245
|
|
|
navicular bone, accessory
|
[NCBI]
|
0.00013559
|
|
|
aneurysmal bone cysts
|
[NCBI]
|
0.00013559
|
|
|
dysplasia epiphysealis hemimelica
|
[NCBI]
|
0.00013559
|
|
|
chondrodysplasia punctata, tibia-metacarpal type
|
[NCBI]
|
0.00013559
|
|
|
CRMO
|
[NCBI]
|
0.000127128
|
|
|
camptomelic syndrome, long-limb type
|
[NCBI]
|
0.000111256
|
|
|
pulmonary hypertension, familial persistent, of the newborn
|
[NCBI]
|
0.000111256
|
|
|
OPTB5
|
[NCBI]
|
0.000104156
|
|
|
LGMD2J
|
[NCBI]
|
0.000104156
|
|
|
MAS
|
[NCBI]
|
9.97004e-05
|
|
|
fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly
|
[NCBI]
|
9.85099e-05
|
|
|
femur-fibula-ulna syndrome
|
[NCBI]
|
9.85099e-05
|
|
|
OSMED
|
[NCBI]
|
9.85099e-05
|
|
|
epidermolysis bullosa dystrophica, pasini type
|
[NCBI]
|
9.38248e-05
|
|
|
GDD
|
[NCBI]
|
8.98224e-05
|
|
|
OGD
|
[NCBI]
|
8.98224e-05
|
|
|
RNS
|
[NCBI]
|
8.63306e-05
|
|
|
acheiropody
|
[NCBI]
|
8.04561e-05
|
|
|
stuve-wiedemann syndrome
|
[NCBI]
|
8.04561e-05
|
|
|
FFS
|
[NCBI]
|
7.79359e-05
|
|
|
paget disease, juvenile
|
[NCBI]
|
7.79359e-05
|
|
|
EDM1
|
[NCBI]
|
7.79359e-05
|
|
|
IHH
|
[NCBI]
|
7.61016e-05
|
|
|
osteogenesis imperfecta, type iii
|
[NCBI]
|
7.56312e-05
|
|
|
osteogenesis imperfecta, type iv
|
[NCBI]
|
7.56312e-05
|
|
|
CIPA
|
[NCBI]
|
7.56312e-05
|
|
|
PPD2
|
[NCBI]
|
7.35087e-05
|
|
|
FMD
|
[NCBI]
|
7.35087e-05
|
|
|
chondrodysplasia punctata, autosomal dominant
|
[NCBI]
|
7.15423e-05
|
|
|
HRPT1
|
[NCBI]
|
6.97111e-05
|
|
|
NPPC
|
[NCBI]
|
6.80538e-05
|
|
|
sacral defect with anterior meningocele
|
[NCBI]
|
6.79982e-05
|
|
|
HFTC
|
[NCBI]
|
6.34411e-05
|
|
|
HCH
|
[NCBI]
|
6.34411e-05
|
|
|
MTS
|
[NCBI]
|
6.34411e-05
|
|
|
hypophosphatasia, infantile
|
[NCBI]
|
6.20829e-05
|
|
|
MATN3
|
[NCBI]
|
5.9558e-05
|
|
|
EGF
|
[NCBI]
|
5.63127e-05
|
|
|
SPARC
|
[NCBI]
|
5.50717e-05
|
|
|
HSAN3
|
[NCBI]
|
5.32191e-05
|
|
|
PTHLH
|
[NCBI]
|
5.16674e-05
|
|
|
COMP
|
[NCBI]
|
5.09769e-05
|
|
|
osteogenesis imperfecta, type iia
|
[NCBI]
|
4.9734e-05
|
|
|
VDR
|
[NCBI]
|
4.81135e-05
|
|
|
TRPS2
|
[NCBI]
|
4.46207e-05
|
|
|
TNFSF11
|
[NCBI]
|
4.37413e-05
|
|
|
ALS1
|
[NCBI]
|
3.98678e-05
|
|
|
SDS
|
[NCBI]
|
3.83099e-05
|
|
|
FGFR3
|
[NCBI]
|
3.82629e-05
|
|
|
PSACH
|
[NCBI]
|
3.73276e-05
|
|
|
osteogenesis imperfecta, type i
|
[NCBI]
|
3.54836e-05
|
|
|
GHR
|
[NCBI]
|
3.46658e-05
|
|
|
EVC2
|
[NCBI]
|
3.40133e-05
|
|
|
WSB1
|
[NCBI]
|
3.40133e-05
|
|
|
COL1A1
|
[NCBI]
|
3.3156e-05
|
|
|
CDLS1
|
[NCBI]
|
3.18277e-05
|
|
|
ACH
|
[NCBI]
|
3.10937e-05
|
|
|
DMP1
|
[NCBI]
|
2.83249e-05
|
|
|
FAM20C
|
[NCBI]
|
2.83249e-05
|
|
|
NPPB
|
[NCBI]
|
2.83249e-05
|
|
|
NPR3
|
[NCBI]
|
2.83249e-05
|
|
|
plasmin inhibitor deficiency
|
[NCBI]
|
2.44203e-05
|
|
|
IL6ST
|
[NCBI]
|
2.19259e-05
|
|
|
DDIT3
|
[NCBI]
|
1.83315e-05
|
|
|
NF1
|
[NCBI]
|
1.8069e-05
|
|
|
TNFRSF6B
|
[NCBI]
|
1.74585e-05
|
|
|
PTHR1
|
[NCBI]
|
1.71909e-05
|
|
|
ACHE
|
[NCBI]
|
1.53913e-05
|
|
|
PHEX
|
[NCBI]
|
1.498e-05
|
|
|
CSF3
|
[NCBI]
|
1.46148e-05
|
|
|
GFAP
|
[NCBI]
|
1.44595e-05
|
|
|
BGN
|
[NCBI]
|
1.44396e-05
|
|
|
IRS1
|
[NCBI]
|
1.31873e-05
|
|
|
VEGF
|
[NCBI]
|
1.28427e-05
|
|
|
ALB
|
[NCBI]
|
1.25396e-05
|
|
|
VIP
|
[NCBI]
|
1.23556e-05
|
|
|
CD36
|
[NCBI]
|
1.16791e-05
|
|
|
phenylketonuria
|
[NCBI]
|
1.13533e-05
|
|
|
PRL
|
[NCBI]
|
1.12907e-05
|
|
|
FGF8
|
[NCBI]
|
1.06553e-05
|
|
|
PPARG
|
[NCBI]
|
9.5439e-06
|
|
|
PTN
|
[NCBI]
|
7.818e-06
|
|
|
LEP
|
[NCBI]
|
7.818e-06
|
|
|
MPO
|
[NCBI]
|
7.54711e-06
|
|
|
BMP4
|
[NCBI]
|
7.32963e-06
|
|
|
FGF2
|
[NCBI]
|
5.97712e-06
|
|
|
NPY
|
[NCBI]
|
5.67553e-06
|
|
|
GPI
|
[NCBI]
|
4.60046e-06
|
|
|
TNF
|
[NCBI]
|
4.36316e-06
|
|
|
PEDF
|
[NCBI]
|
4.32326e-06
|
|
|
GAPDH
|
[NCBI]
|
3.85964e-06
|
|
|
AKR1B1
|
[NCBI]
|
3.31997e-06
|
|
|
HDC
|
[NCBI]
|
2.50176e-06
|
|
|
KLK3
|
[NCBI]
|
2.31341e-06
|
|
|
PCNA
|
[NCBI]
|
2.14964e-06
|
|
|
GIP
|
[NCBI]
|
2.00733e-06
|
|
|
GHRH
|
[NCBI]
|
1.90697e-06
|
|
|
SHH
|
[NCBI]
|
1.63419e-06
|
|
|
OSM
|
[NCBI]
|
1.50486e-06
|
|
|
HGF
|
[NCBI]
|
1.30108e-06
|
|
|
CD
|
[NCBI]
|
1.09692e-06
|
|
|
RA
|
[NCBI]
|
9.17504e-07
|
|
|
APOE
|
[NCBI]
|
9.0816e-07
|
|
|
SHBG
|
[NCBI]
|
7.92509e-07
|
|
|
SOD2
|
[NCBI]
|
6.84139e-07
|
|
|
CTGF
|
[NCBI]
|
4.66255e-07
|
|
|
AR
|
[NCBI]
|
6.61542e-08
|
|
|
AHR
|
[NCBI]
|
7.1299e-09
|
|