|
OMIM |
Link |
Information gain |
01 |
|
PTH
|
[NCBI]
|
0.00847904
|
|
|
BMND3
|
[NCBI]
|
0.00610333
|
|
|
VDR
|
[NCBI]
|
0.00389625
|
|
|
IS1
|
[NCBI]
|
0.00225102
|
|
|
BMND5
|
[NCBI]
|
0.00218456
|
|
|
BMND2
|
[NCBI]
|
0.00218456
|
|
|
TNFRSF11B
|
[NCBI]
|
0.00209175
|
|
|
osteogenesis imperfecta, type v
|
[NCBI]
|
0.00181985
|
|
|
osteogenesis imperfecta, type vi
|
[NCBI]
|
0.00181985
|
|
|
RA
|
[NCBI]
|
0.00178804
|
|
|
osteoporosis
|
[NCBI]
|
0.00169202
|
|
|
BMND1
|
[NCBI]
|
0.00132389
|
|
|
BMND7
|
[NCBI]
|
0.00108846
|
|
|
BMND4
|
[NCBI]
|
0.00108846
|
|
|
BMND6
|
[NCBI]
|
0.00108846
|
|
|
BGLAP
|
[NCBI]
|
0.000735693
|
|
|
stature quantitative trait locus 3
|
[NCBI]
|
0.000660042
|
|
|
ACP5
|
[NCBI]
|
0.000643922
|
|
|
CMDR
|
[NCBI]
|
0.000612338
|
|
|
torus palatinus and torus mandibularis
|
[NCBI]
|
0.000612338
|
|
|
diarrhea 2, with microvillous atrophy
|
[NCBI]
|
0.000543053
|
|
|
osteoporosis, juvenile
|
[NCBI]
|
0.000444194
|
|
|
OPPG
|
[NCBI]
|
0.000335764
|
|
|
osteogenesis imperfecta, type i
|
[NCBI]
|
0.000316353
|
|
|
CD
|
[NCBI]
|
0.000311566
|
|
|
osteogenesis imperfecta, type iv
|
[NCBI]
|
0.000290661
|
|
|
vitamin d-dependent rickets, type ii
|
[NCBI]
|
0.000288866
|
|
|
osteogenesis imperfecta, type iii
|
[NCBI]
|
0.000279371
|
|
|
EGF
|
[NCBI]
|
0.000259497
|
|
|
SHBG
|
[NCBI]
|
0.000187766
|
|
|
hyperostosis corticalis generalisata
|
[NCBI]
|
0.00018334
|
|
|
CF
|
[NCBI]
|
0.000181439
|
|
|
VEGF
|
[NCBI]
|
0.000173725
|
|
|
CRC
|
[NCBI]
|
0.000161214
|
|
|
LRP5
|
[NCBI]
|
0.000154462
|
|
|
AD
|
[NCBI]
|
0.000153853
|
|
|
ESR1
|
[NCBI]
|
0.000144886
|
|
|
HCA2
|
[NCBI]
|
0.000127175
|
|
|
BOCD
|
[NCBI]
|
0.000108555
|
|
|
TNF
|
[NCBI]
|
0.000108292
|
|
|
CASR
|
[NCBI]
|
0.000108136
|
|
|
brittle bone disorder
|
[NCBI]
|
0.000101571
|
|
|
hypouricemia, hypercalcinuria, and decreased bone density
|
[NCBI]
|
0.000101571
|
|
|
chondrodysplasia, lethal, with long bone angulation and mixed bone density
|
[NCBI]
|
0.000101571
|
|
|
polycystic bone disease
|
[NCBI]
|
0.000101571
|
|
|
van buchem disease, type 2
|
[NCBI]
|
0.000101571
|
|
|
CYP19A1
|
[NCBI]
|
8.78899e-05
|
|
|
diabetes insipidus, neurohypophyseal type
|
[NCBI]
|
8.41731e-05
|
|
|
NPY
|
[NCBI]
|
8.22055e-05
|
|
|
SOST
|
[NCBI]
|
7.94596e-05
|
|
|
GFAP
|
[NCBI]
|
7.78215e-05
|
|
|
EPO
|
[NCBI]
|
7.56462e-05
|
|
|
CALCR
|
[NCBI]
|
7.51345e-05
|
|
|
rapadilino syndrome
|
[NCBI]
|
7.39232e-05
|
|
|
PCNA
|
[NCBI]
|
6.36674e-05
|
|
|
PWS
|
[NCBI]
|
6.33861e-05
|
|
|
OPTA1
|
[NCBI]
|
5.68847e-05
|
|
|
osteogenesis imperfecta, type vii
|
[NCBI]
|
5.68847e-05
|
|
|
AIS
|
[NCBI]
|
5.53537e-05
|
|
|
osteolysis, hereditary multicentric
|
[NCBI]
|
5.19487e-05
|
|
|
insulin-like growth factor i deficiency
|
[NCBI]
|
5.19487e-05
|
|
|
hyperostosis corticalis generalisata, benign form of worth, with torus palatinus
|
[NCBI]
|
5.19487e-05
|
|
|
BGN
|
[NCBI]
|
4.90296e-05
|
|
|
MONA
|
[NCBI]
|
4.80408e-05
|
|
|
EVR4
|
[NCBI]
|
4.80408e-05
|
|
|
HOMG2
|
[NCBI]
|
4.80408e-05
|
|
|
paget disease, juvenile
|
[NCBI]
|
4.80408e-05
|
|
|
KLK3
|
[NCBI]
|
4.74883e-05
|
|
|
TNFRSF1B
|
[NCBI]
|
4.72675e-05
|
|
|
PD
|
[NCBI]
|
4.52173e-05
|
|
|
weill-marchesani syndrome, autosomal recessive
|
[NCBI]
|
4.48122e-05
|
|
|
winchester syndrome
|
[NCBI]
|
4.48122e-05
|
|
|
LPL
|
[NCBI]
|
4.35495e-05
|
|
|
SLE
|
[NCBI]
|
4.11272e-05
|
|
|
MDD
|
[NCBI]
|
4.00065e-05
|
|
|
ALOX15
|
[NCBI]
|
3.97208e-05
|
|
|
COL1A1
|
[NCBI]
|
3.60254e-05
|
|
|
HSS
|
[NCBI]
|
3.56966e-05
|
|
|
lymphoma, non-hodgkin, familial
|
[NCBI]
|
3.26885e-05
|
|
|
BMP2
|
[NCBI]
|
3.25699e-05
|
|
|
NPPB
|
[NCBI]
|
3.15712e-05
|
|
|
RUNX2
|
[NCBI]
|
3.12582e-05
|
|
|
hypogonadotropic hypogonadism
|
[NCBI]
|
3.12012e-05
|
|
|
trichodentoosseous syndrome
|
[NCBI]
|
3.10371e-05
|
|
|
mucolipidosis iiia
|
[NCBI]
|
3.10371e-05
|
|
|
dent disease 1
|
[NCBI]
|
2.9731e-05
|
|
|
SOST
|
[NCBI]
|
2.9731e-05
|
|
|
hypophosphatasia, adult type
|
[NCBI]
|
2.9731e-05
|
|
|
CAT
|
[NCBI]
|
2.96762e-05
|
|
|
CFTR
|
[NCBI]
|
2.95219e-05
|
|
|
PRL
|
[NCBI]
|
2.91024e-05
|
|
|
CMDD
|
[NCBI]
|
2.85205e-05
|
|
|
IL6
|
[NCBI]
|
2.83514e-05
|
|
|
LEPR
|
[NCBI]
|
2.77699e-05
|
|
|
EVR1
|
[NCBI]
|
2.73937e-05
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
2.63678e-05
|
|
|
BGS
|
[NCBI]
|
2.63407e-05
|
|
|
SCN1
|
[NCBI]
|
2.63407e-05
|
|
|
camurati-engelmann disease
|
[NCBI]
|
2.63407e-05
|
|
|
ALOX5
|
[NCBI]
|
2.61567e-05
|
|
|
TNFSF6
|
[NCBI]
|
2.59642e-05
|
|
|
TTDP
|
[NCBI]
|
2.53533e-05
|
|
|
HRPT1
|
[NCBI]
|
2.53533e-05
|
|
|
MAS
|
[NCBI]
|
2.38056e-05
|
|
|
hyperoxaluria, primary, type i
|
[NCBI]
|
2.35486e-05
|
|
|
CXORF15
|
[NCBI]
|
2.29395e-05
|
|
|
SPP1
|
[NCBI]
|
2.26968e-05
|
|
|
IL1RN
|
[NCBI]
|
2.25539e-05
|
|
|
ODDD
|
[NCBI]
|
2.04816e-05
|
|
|
CTSK
|
[NCBI]
|
2.02742e-05
|
|
|
adenylyl cyclase, soluble
|
[NCBI]
|
1.98729e-05
|
|
|
ATF4
|
[NCBI]
|
1.98729e-05
|
|
|
GDF2
|
[NCBI]
|
1.98581e-05
|
|
|
PDLIM4
|
[NCBI]
|
1.98581e-05
|
|
|
LEP
|
[NCBI]
|
1.81831e-05
|
|
|
PLCG2
|
[NCBI]
|
1.78683e-05
|
|
|
homocysteinemia
|
[NCBI]
|
1.73914e-05
|
|
|
hypophosphatasia, infantile
|
[NCBI]
|
1.73914e-05
|
|
|
graves disease
|
[NCBI]
|
1.73914e-05
|
|
|
FMF
|
[NCBI]
|
1.6895e-05
|
|
|
PTHR1
|
[NCBI]
|
1.68407e-05
|
|
|
HIVEP3
|
[NCBI]
|
1.63967e-05
|
|
|
THBS2
|
[NCBI]
|
1.63967e-05
|
|
|
PLXNA2
|
[NCBI]
|
1.63967e-05
|
|
|
temporal arteritis
|
[NCBI]
|
1.63344e-05
|
|
|
PTHLH
|
[NCBI]
|
1.59553e-05
|
|
|
GH1
|
[NCBI]
|
1.59474e-05
|
|
|
VAV3
|
[NCBI]
|
1.52305e-05
|
|
|
DLX3
|
[NCBI]
|
1.52305e-05
|
|
|
CRTAP
|
[NCBI]
|
1.52305e-05
|
|
|
FIH
|
[NCBI]
|
1.44391e-05
|
|
|
TNFSF11
|
[NCBI]
|
1.4333e-05
|
|
|
DMP1
|
[NCBI]
|
1.4266e-05
|
|
|
IL1R1
|
[NCBI]
|
1.4266e-05
|
|
|
growth hormone insensitivity syndrome
|
[NCBI]
|
1.31923e-05
|
|
|
SEMA7A
|
[NCBI]
|
1.2731e-05
|
|
|
HBB
|
[NCBI]
|
1.24459e-05
|
|
|
FZD4
|
[NCBI]
|
1.21003e-05
|
|
|
BMP6
|
[NCBI]
|
1.21003e-05
|
|
|
RTS
|
[NCBI]
|
1.17168e-05
|
|
|
IGF1
|
[NCBI]
|
1.16515e-05
|
|
|
GAPDH
|
[NCBI]
|
1.14792e-05
|
|
|
WNT3A
|
[NCBI]
|
1.10261e-05
|
|
|
SYK
|
[NCBI]
|
1.10261e-05
|
|
|
CLCN7
|
[NCBI]
|
1.05615e-05
|
|
|
TF
|
[NCBI]
|
1.05502e-05
|
|
|
NPS
|
[NCBI]
|
1.04196e-05
|
|
|
TCIRG1
|
[NCBI]
|
1.01351e-05
|
|
|
GGCX
|
[NCBI]
|
9.37628e-06
|
|
|
CNR1
|
[NCBI]
|
9.03591e-06
|
|
|
PLIN
|
[NCBI]
|
9.03591e-06
|
|
|
ADIPOR1
|
[NCBI]
|
9.03591e-06
|
|
|
IL6R
|
[NCBI]
|
8.41848e-06
|
|
|
BMP7
|
[NCBI]
|
8.13692e-06
|
|
|
NFATC1
|
[NCBI]
|
7.87103e-06
|
|
|
HSD11B1
|
[NCBI]
|
7.87103e-06
|
|
|
GHSR
|
[NCBI]
|
7.38052e-06
|
|
|
FOXC2
|
[NCBI]
|
7.38052e-06
|
|
|
DLK1
|
[NCBI]
|
7.38052e-06
|
|
|
GHRHR
|
[NCBI]
|
7.38052e-06
|
|
|
PPARA
|
[NCBI]
|
7.32417e-06
|
|
|
NIDDM
|
[NCBI]
|
6.91392e-06
|
|
|
FGF4
|
[NCBI]
|
6.53374e-06
|
|
|
SP7
|
[NCBI]
|
6.53374e-06
|
|
|
SFRP1
|
[NCBI]
|
6.34505e-06
|
|
|
COMP
|
[NCBI]
|
6.32823e-06
|
|
|
KL
|
[NCBI]
|
6.16424e-06
|
|
|
TNFRSF6B
|
[NCBI]
|
6.16424e-06
|
|
|
INPP5D
|
[NCBI]
|
6.16424e-06
|
|
|
PROS1
|
[NCBI]
|
5.82412e-06
|
|
|
APOE
|
[NCBI]
|
5.81666e-06
|
|
|
menkes disease
|
[NCBI]
|
5.77702e-06
|
|
|
IL1B
|
[NCBI]
|
5.66389e-06
|
|
|
ERCC2
|
[NCBI]
|
5.50965e-06
|
|
|
ALPL
|
[NCBI]
|
5.50965e-06
|
|
|
BMP4
|
[NCBI]
|
5.47022e-06
|
|
|
AR
|
[NCBI]
|
5.45248e-06
|
|
|
PYY
|
[NCBI]
|
5.26747e-06
|
|
|
PTN
|
[NCBI]
|
5.07987e-06
|
|
|
PHEX
|
[NCBI]
|
4.8168e-06
|
|
|
XPA
|
[NCBI]
|
4.69193e-06
|
|
|
CCD
|
[NCBI]
|
4.65578e-06
|
|
|
FY
|
[NCBI]
|
4.34063e-06
|
|
|
LIFR
|
[NCBI]
|
4.23068e-06
|
|
|
POLG
|
[NCBI]
|
3.92001e-06
|
|
|
ALB
|
[NCBI]
|
3.74802e-06
|
|
|
GHR
|
[NCBI]
|
3.67125e-06
|
|
|
ACE
|
[NCBI]
|
3.58904e-06
|
|
|
MSTN
|
[NCBI]
|
3.45827e-06
|
|
|
APS1
|
[NCBI]
|
2.82939e-06
|
|
|
fabry disease
|
[NCBI]
|
2.73059e-06
|
|
|
CVID
|
[NCBI]
|
2.61054e-06
|
|
|
ITGB3
|
[NCBI]
|
2.50774e-06
|
|
|
PGR
|
[NCBI]
|
2.48729e-06
|
|
|
AHR
|
[NCBI]
|
2.43121e-06
|
|
|
NMU
|
[NCBI]
|
2.27117e-06
|
|
|
MFS
|
[NCBI]
|
2.27066e-06
|
|
|
RTT
|
[NCBI]
|
2.06303e-06
|
|
|
OSM
|
[NCBI]
|
1.71056e-06
|
|
|
STC1
|
[NCBI]
|
1.5131e-06
|
|
|
GJA1
|
[NCBI]
|
1.43773e-06
|
|
|
GNRH1
|
[NCBI]
|
1.38952e-06
|
|
|
LCT
|
[NCBI]
|
1.32571e-06
|
|
|
INS
|
[NCBI]
|
1.23639e-06
|
|
|
PAEP
|
[NCBI]
|
9.22678e-07
|
|
|
TNFSF10
|
[NCBI]
|
8.16733e-07
|
|
|
CALCRL
|
[NCBI]
|
6.80863e-07
|
|
|
LAM
|
[NCBI]
|
6.49266e-07
|
|
|
CTGF
|
[NCBI]
|
6.18135e-07
|
|
|
PPARG
|
[NCBI]
|
5.22409e-07
|
|
|
HDC
|
[NCBI]
|
4.73588e-07
|
|
|
MITF
|
[NCBI]
|
3.6154e-07
|
|
|
IGFALS
|
[NCBI]
|
3.47501e-07
|
|
|
STAT1
|
[NCBI]
|
1.41656e-07
|
|
|
phenylketonuria
|
[NCBI]
|
1.30408e-07
|
|
|
COMT
|
[NCBI]
|
1.10673e-07
|
|
|
LRP1
|
[NCBI]
|
1.02066e-07
|
|
|
PTEN
|
[NCBI]
|
9.15164e-08
|
|
|
FGF2
|
[NCBI]
|
9.15164e-08
|
|
|
FGFR2
|
[NCBI]
|
4.03156e-08
|
|
|
GHRH
|
[NCBI]
|
1.64389e-08
|
|
|
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency
|
[NCBI]
|
8.21286e-09
|
|
|
polycystic kidneys
|
[NCBI]
|
3.29895e-09
|
|