|
OMIM |
Link |
Information gain |
01 |
|
GO
|
[NCBI]
|
0.00696975
|
|
|
PTH
|
[NCBI]
|
0.00579569
|
|
|
singleton-merten syndrome
|
[NCBI]
|
0.00211553
|
|
|
TNFRSF11B
|
[NCBI]
|
0.00208964
|
|
|
VDR
|
[NCBI]
|
0.00202519
|
|
|
OPPG
|
[NCBI]
|
0.00126995
|
|
|
osteoporosis, juvenile
|
[NCBI]
|
0.00126995
|
|
|
RA
|
[NCBI]
|
0.00124589
|
|
|
BMND7
|
[NCBI]
|
0.00105062
|
|
|
BMND2
|
[NCBI]
|
0.00105062
|
|
|
osteoporosis
|
[NCBI]
|
0.000756725
|
|
|
bruck syndrome 1
|
[NCBI]
|
0.000657993
|
|
|
BGLAP
|
[NCBI]
|
0.000438867
|
|
|
ACP5
|
[NCBI]
|
0.000347843
|
|
|
VEGF
|
[NCBI]
|
0.000256349
|
|
|
CD
|
[NCBI]
|
0.000242114
|
|
|
BMND1
|
[NCBI]
|
0.000205781
|
|
|
TNFSF11
|
[NCBI]
|
0.000201618
|
|
|
spondyloocular syndrome, autosomal recessive
|
[NCBI]
|
0.000181965
|
|
|
prader-willi habitus, osteopenia, and camptodactyly
|
[NCBI]
|
0.000181965
|
|
|
LRP5
|
[NCBI]
|
0.00015786
|
|
|
EGF
|
[NCBI]
|
0.000143991
|
|
|
CYP19A1
|
[NCBI]
|
0.000126066
|
|
|
winchester syndrome
|
[NCBI]
|
0.000105097
|
|
|
ESR1
|
[NCBI]
|
9.54373e-05
|
|
|
ADCAD2
|
[NCBI]
|
9.09575e-05
|
|
|
macroepiphyseal dysplasia with osteoporosis, wrinkled skin, and aged appearance
|
[NCBI]
|
9.09575e-05
|
|
|
premature aging syndrome, okamoto type
|
[NCBI]
|
9.09575e-05
|
|
|
tendons, extensor, of fingers, anomalous insertion of
|
[NCBI]
|
9.09575e-05
|
|
|
OOCH
|
[NCBI]
|
9.09575e-05
|
|
|
BGN
|
[NCBI]
|
8.68051e-05
|
|
|
paget disease, juvenile
|
[NCBI]
|
8.50698e-05
|
|
|
PCNA
|
[NCBI]
|
7.81952e-05
|
|
|
KLK3
|
[NCBI]
|
7.60485e-05
|
|
|
CMDD
|
[NCBI]
|
7.6028e-05
|
|
|
BMP2
|
[NCBI]
|
7.27505e-05
|
|
|
LPI
|
[NCBI]
|
7.18939e-05
|
|
|
bruck syndrome 2
|
[NCBI]
|
6.85442e-05
|
|
|
microcephalic primordial dwarfism, toriello type
|
[NCBI]
|
6.85442e-05
|
|
|
ataxia-microcephaly-cataract syndrome
|
[NCBI]
|
6.85442e-05
|
|
|
van buchem disease, type 2
|
[NCBI]
|
6.85442e-05
|
|
|
homocysteinemia
|
[NCBI]
|
6.45066e-05
|
|
|
EPO
|
[NCBI]
|
6.35671e-05
|
|
|
CALCR
|
[NCBI]
|
6.15632e-05
|
|
|
SHBG
|
[NCBI]
|
6.02253e-05
|
|
|
mental retardation, x-linked, snyder-robinson type
|
[NCBI]
|
6.01213e-05
|
|
|
CELIAC4
|
[NCBI]
|
5.46723e-05
|
|
|
angiolipomatosis, familial
|
[NCBI]
|
5.46723e-05
|
|
|
BMND8
|
[NCBI]
|
5.43217e-05
|
|
|
PDLIM4
|
[NCBI]
|
5.43217e-05
|
|
|
ALOX15
|
[NCBI]
|
5.43217e-05
|
|
|
OPTA1
|
[NCBI]
|
5.06356e-05
|
|
|
EVR4
|
[NCBI]
|
4.74309e-05
|
|
|
CTSK
|
[NCBI]
|
4.69154e-05
|
|
|
nephrosialidosis
|
[NCBI]
|
4.47758e-05
|
|
|
cataract, microcephaly, failure to thrive, kyphoscoliosis syndrome
|
[NCBI]
|
4.47758e-05
|
|
|
GDD
|
[NCBI]
|
4.25113e-05
|
|
|
WARBM
|
[NCBI]
|
4.25113e-05
|
|
|
TNFRSF1B
|
[NCBI]
|
4.19951e-05
|
|
|
TICAM2
|
[NCBI]
|
4.05831e-05
|
|
|
SP7
|
[NCBI]
|
4.05831e-05
|
|
|
TRPV5
|
[NCBI]
|
4.05831e-05
|
|
|
IL7
|
[NCBI]
|
4.05831e-05
|
|
|
atransferrinemia
|
[NCBI]
|
4.0539e-05
|
|
|
martsolf syndrome
|
[NCBI]
|
4.0539e-05
|
|
|
hyperostosis corticalis generalisata, benign form of worth, with torus palatinus
|
[NCBI]
|
3.87934e-05
|
|
|
weill-marchesani syndrome, autosomal recessive
|
[NCBI]
|
3.87934e-05
|
|
|
HHRH
|
[NCBI]
|
3.7229e-05
|
|
|
TNF
|
[NCBI]
|
3.60826e-05
|
|
|
WSS
|
[NCBI]
|
3.58125e-05
|
|
|
hyperostosis corticalis generalisata
|
[NCBI]
|
3.58125e-05
|
|
|
PTGER4
|
[NCBI]
|
3.54238e-05
|
|
|
SMPD3
|
[NCBI]
|
3.54238e-05
|
|
|
COL1A1
|
[NCBI]
|
3.31465e-05
|
|
|
PRL
|
[NCBI]
|
3.29672e-05
|
|
|
CACP
|
[NCBI]
|
3.22309e-05
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
3.21131e-05
|
|
|
CYP2R1
|
[NCBI]
|
3.20881e-05
|
|
|
COFS1
|
[NCBI]
|
3.12088e-05
|
|
|
cutis laxa, autosomal recessive, type ii
|
[NCBI]
|
3.12088e-05
|
|
|
SATB2
|
[NCBI]
|
2.96185e-05
|
|
|
SLC34A1
|
[NCBI]
|
2.96185e-05
|
|
|
LRP6
|
[NCBI]
|
2.96185e-05
|
|
|
HSAN2
|
[NCBI]
|
2.93595e-05
|
|
|
CASR
|
[NCBI]
|
2.80591e-05
|
|
|
PLOSL
|
[NCBI]
|
2.77235e-05
|
|
|
SOST
|
[NCBI]
|
2.77235e-05
|
|
|
SCN1
|
[NCBI]
|
2.77235e-05
|
|
|
IL6
|
[NCBI]
|
2.74518e-05
|
|
|
MG
|
[NCBI]
|
2.62813e-05
|
|
|
diabetes insipidus, neurohypophyseal type
|
[NCBI]
|
2.6259e-05
|
|
|
TYROBP
|
[NCBI]
|
2.60367e-05
|
|
|
TREM2
|
[NCBI]
|
2.60367e-05
|
|
|
PPP3CA
|
[NCBI]
|
2.60367e-05
|
|
|
INPP5D
|
[NCBI]
|
2.46539e-05
|
|
|
FZD4
|
[NCBI]
|
2.46539e-05
|
|
|
EVR1
|
[NCBI]
|
2.37299e-05
|
|
|
TRAF6
|
[NCBI]
|
2.34502e-05
|
|
|
hyperimmunoglobulin e recurrent infection syndrome, autosomal dominant
|
[NCBI]
|
2.31656e-05
|
|
|
CAT
|
[NCBI]
|
2.29126e-05
|
|
|
SOST
|
[NCBI]
|
2.23855e-05
|
|
|
NR1I2
|
[NCBI]
|
2.1999e-05
|
|
|
camurati-engelmann disease
|
[NCBI]
|
2.16049e-05
|
|
|
niemann-pick disease, type a
|
[NCBI]
|
2.06601e-05
|
|
|
lactase persistence
|
[NCBI]
|
2.06601e-05
|
|
|
PLIN
|
[NCBI]
|
2.05691e-05
|
|
|
IL6R
|
[NCBI]
|
2.05691e-05
|
|
|
LEPR
|
[NCBI]
|
2.02894e-05
|
|
|
OCRL
|
[NCBI]
|
1.97808e-05
|
|
|
FPLD2
|
[NCBI]
|
1.97808e-05
|
|
|
ALOX5
|
[NCBI]
|
1.90586e-05
|
|
|
CALCA
|
[NCBI]
|
1.90586e-05
|
|
|
vitamin d-dependent rickets, type ii
|
[NCBI]
|
1.85683e-05
|
|
|
ehlers-danlos syndrome, type i
|
[NCBI]
|
1.81895e-05
|
|
|
MAPK3
|
[NCBI]
|
1.77691e-05
|
|
|
KL
|
[NCBI]
|
1.71895e-05
|
|
|
IL1RN
|
[NCBI]
|
1.66466e-05
|
|
|
VIP
|
[NCBI]
|
1.63559e-05
|
|
|
FOXC2
|
[NCBI]
|
1.61362e-05
|
|
|
PD
|
[NCBI]
|
1.59244e-05
|
|
|
IL1B
|
[NCBI]
|
1.56549e-05
|
|
|
GNRH1
|
[NCBI]
|
1.53116e-05
|
|
|
NOG
|
[NCBI]
|
1.51998e-05
|
|
|
TNFSF6
|
[NCBI]
|
1.50871e-05
|
|
|
SFRP1
|
[NCBI]
|
1.47684e-05
|
|
|
LCT
|
[NCBI]
|
1.47684e-05
|
|
|
homocystinuria
|
[NCBI]
|
1.41185e-05
|
|
|
PTK2B
|
[NCBI]
|
1.35962e-05
|
|
|
RUNX2
|
[NCBI]
|
1.35962e-05
|
|
|
costello syndrome
|
[NCBI]
|
1.33783e-05
|
|
|
osteogenesis imperfecta, type iia
|
[NCBI]
|
1.20113e-05
|
|
|
NIDDM
|
[NCBI]
|
1.18004e-05
|
|
|
BMP4
|
[NCBI]
|
1.13928e-05
|
|
|
GCCR
|
[NCBI]
|
1.08651e-05
|
|
|
IRS1
|
[NCBI]
|
1.06148e-05
|
|
|
ITGB2
|
[NCBI]
|
9.91238e-06
|
|
|
ABL1
|
[NCBI]
|
9.69291e-06
|
|
|
UCP3
|
[NCBI]
|
9.07344e-06
|
|
|
CALCRL
|
[NCBI]
|
8.3273e-06
|
|
|
hypogonadotropic hypogonadism
|
[NCBI]
|
7.94238e-06
|
|
|
AQP2
|
[NCBI]
|
7.81902e-06
|
|
|
osteogenesis imperfecta, type i
|
[NCBI]
|
7.80876e-06
|
|
|
FMF
|
[NCBI]
|
7.67367e-06
|
|
|
menkes disease
|
[NCBI]
|
7.54827e-06
|
|
|
TLR9
|
[NCBI]
|
7.50163e-06
|
|
|
KAL1
|
[NCBI]
|
7.50163e-06
|
|
|
SDS
|
[NCBI]
|
7.05292e-06
|
|
|
GH1
|
[NCBI]
|
6.77391e-06
|
|
|
temporal arteritis
|
[NCBI]
|
6.57897e-06
|
|
|
IL4
|
[NCBI]
|
6.37706e-06
|
|
|
wilson disease
|
[NCBI]
|
5.00367e-06
|
|
|
TNFSF10
|
[NCBI]
|
4.45222e-06
|
|
|
fabry disease
|
[NCBI]
|
4.34564e-06
|
|
|
COL1A2
|
[NCBI]
|
4.29703e-06
|
|
|
APOE
|
[NCBI]
|
3.48745e-06
|
|
|
CFTR
|
[NCBI]
|
3.48384e-06
|
|
|
AR
|
[NCBI]
|
3.46612e-06
|
|
|
SPP1
|
[NCBI]
|
3.21118e-06
|
|
|
CF
|
[NCBI]
|
2.6553e-06
|
|
|
LRP1
|
[NCBI]
|
1.76824e-06
|
|
|
HDC
|
[NCBI]
|
1.57826e-06
|
|
|
LEP
|
[NCBI]
|
1.47181e-06
|
|
|
TF
|
[NCBI]
|
1.30672e-06
|
|
|
COMT
|
[NCBI]
|
1.21246e-06
|
|
|
CNTF
|
[NCBI]
|
6.67296e-07
|
|
|
CPI
|
[NCBI]
|
6.50316e-07
|
|
|
ALB
|
[NCBI]
|
5.02365e-07
|
|
|
AHR
|
[NCBI]
|
3.49562e-07
|
|
|
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency
|
[NCBI]
|
1.22116e-07
|
|
|
HFE
|
[NCBI]
|
8.22308e-08
|
|
|
GIP
|
[NCBI]
|
5.66384e-08
|
|
|
PTHLH
|
[NCBI]
|
4.68883e-08
|
|
|
GHRH
|
[NCBI]
|
1.57141e-08
|
|
|
TP53
|
[NCBI]
|
1.11796e-08
|
|
|
CP
|
[NCBI]
|
1.11796e-08
|
|
|
SLE
|
[NCBI]
|
9.63023e-09
|
|
|
MDD
|
[NCBI]
|
4.406e-09
|
|
|
PTK2
|
[NCBI]
|
2.20445e-09
|
|