|
OMIM |
Link |
Information gain |
01 |
|
RA
|
[NCBI]
|
0.0264879
|
|
|
marden-walker syndrome
|
[NCBI]
|
0.00356858
|
|
|
DA5
|
[NCBI]
|
0.00181564
|
|
|
GO
|
[NCBI]
|
0.00163245
|
|
|
muscular dystrophy, congenital, producing arthrogryposis
|
[NCBI]
|
0.0012789
|
|
|
SPOAN
|
[NCBI]
|
0.0012789
|
|
|
NLS
|
[NCBI]
|
0.00122588
|
|
|
leri pleonosteosis
|
[NCBI]
|
0.000968636
|
|
|
synostosis, carpal, with dysplastic elbow joints and brachydactyly
|
[NCBI]
|
0.000968636
|
|
|
SLE
|
[NCBI]
|
0.000875481
|
|
|
VDEGS
|
[NCBI]
|
0.000776494
|
|
|
bruck syndrome 1
|
[NCBI]
|
0.000776494
|
|
|
BWCNS
|
[NCBI]
|
0.000720545
|
|
|
porokeratosis of mibelli
|
[NCBI]
|
0.000676108
|
|
|
acetabular dysplasia
|
[NCBI]
|
0.000639279
|
|
|
larsen syndrome, recessive
|
[NCBI]
|
0.000639279
|
|
|
laurin-sandrow syndrome
|
[NCBI]
|
0.000607856
|
|
|
AMCN
|
[NCBI]
|
0.000580475
|
|
|
ear, patella, short stature syndrome
|
[NCBI]
|
0.000534496
|
|
|
AD
|
[NCBI]
|
0.000374032
|
|
|
COMP
|
[NCBI]
|
0.000314712
|
|
|
MADA
|
[NCBI]
|
0.000144644
|
|
|
microcephalic primordial dwarfism, toriello type
|
[NCBI]
|
0.000126136
|
|
|
uruguay faciocardiomusculoskeletal syndrome
|
[NCBI]
|
0.000126136
|
|
|
megarbane syndrome
|
[NCBI]
|
0.000126136
|
|
|
SYNS1
|
[NCBI]
|
0.000107531
|
|
|
TNFRSF11B
|
[NCBI]
|
9.42559e-05
|
|
|
COFS1
|
[NCBI]
|
9.36199e-05
|
|
|
NOG
|
[NCBI]
|
9.31821e-05
|
|
|
CACP
|
[NCBI]
|
8.97442e-05
|
|
|
GDF5
|
[NCBI]
|
8.84706e-05
|
|
|
ataxia-microcephaly-cataract syndrome
|
[NCBI]
|
8.71902e-05
|
|
|
larsen-like syndrome, lethal type
|
[NCBI]
|
8.71902e-05
|
|
|
martsolf syndrome
|
[NCBI]
|
8.71902e-05
|
|
|
retinopathy, pigmentary, and mental retardation
|
[NCBI]
|
8.71902e-05
|
|
|
STL2
|
[NCBI]
|
8.71902e-05
|
|
|
holoprosencephaly with fetal akinesia/hypokinesia sequence
|
[NCBI]
|
8.71902e-05
|
|
|
PPAC
|
[NCBI]
|
8.28292e-05
|
|
|
OSM
|
[NCBI]
|
7.81289e-05
|
|
|
STL1
|
[NCBI]
|
7.68101e-05
|
|
|
kniest-like dysplasia with pursed lips and ectopia lentis
|
[NCBI]
|
7.26972e-05
|
|
|
psoriatic arthritis, susceptibility to
|
[NCBI]
|
7.26972e-05
|
|
|
cataract, microcephaly, failure to thrive, kyphoscoliosis syndrome
|
[NCBI]
|
7.26972e-05
|
|
|
STL3
|
[NCBI]
|
7.26972e-05
|
|
|
AOIII
|
[NCBI]
|
7.26972e-05
|
|
|
CILP
|
[NCBI]
|
6.64921e-05
|
|
|
microcephaly with chemotactic defect and transient hypogammaglobulinemia
|
[NCBI]
|
6.34017e-05
|
|
|
TNF
|
[NCBI]
|
6.25807e-05
|
|
|
ehlers-danlos syndrome, type iii
|
[NCBI]
|
5.65748e-05
|
|
|
EDM4
|
[NCBI]
|
5.65748e-05
|
|
|
ADORA3
|
[NCBI]
|
5.38428e-05
|
|
|
PRG4
|
[NCBI]
|
5.24375e-05
|
|
|
boomerang dysplasia
|
[NCBI]
|
5.12018e-05
|
|
|
IHH
|
[NCBI]
|
5.09279e-05
|
|
|
IL10
|
[NCBI]
|
4.8906e-05
|
|
|
chondrodysplasia, grebe type
|
[NCBI]
|
4.67896e-05
|
|
|
WSS
|
[NCBI]
|
4.67896e-05
|
|
|
WARBM
|
[NCBI]
|
4.67896e-05
|
|
|
spondylocarpotarsal synostosis syndrome
|
[NCBI]
|
4.67896e-05
|
|
|
ADAMTS5
|
[NCBI]
|
4.33104e-05
|
|
|
sc phocomelia syndrome
|
[NCBI]
|
4.30601e-05
|
|
|
AOI
|
[NCBI]
|
3.98412e-05
|
|
|
AMC
|
[NCBI]
|
3.88328e-05
|
|
|
MOX2
|
[NCBI]
|
3.71038e-05
|
|
|
GDF6
|
[NCBI]
|
3.71038e-05
|
|
|
VEGF
|
[NCBI]
|
3.54724e-05
|
|
|
CD69
|
[NCBI]
|
3.52885e-05
|
|
|
GDF7
|
[NCBI]
|
3.52885e-05
|
|
|
stuve-wiedemann syndrome
|
[NCBI]
|
3.45125e-05
|
|
|
ATS
|
[NCBI]
|
3.45125e-05
|
|
|
IL32
|
[NCBI]
|
3.38428e-05
|
|
|
SPP1
|
[NCBI]
|
3.36765e-05
|
|
|
EDM1
|
[NCBI]
|
3.22652e-05
|
|
|
ERRFI1
|
[NCBI]
|
3.16133e-05
|
|
|
FSTL1
|
[NCBI]
|
3.16133e-05
|
|
|
HLA-DRB1
|
[NCBI]
|
3.07151e-05
|
|
|
FLNB
|
[NCBI]
|
2.92007e-05
|
|
|
COL11A1
|
[NCBI]
|
2.92007e-05
|
|
|
SYM1
|
[NCBI]
|
2.83838e-05
|
|
|
IL1RN
|
[NCBI]
|
2.7953e-05
|
|
|
PGF
|
[NCBI]
|
2.68924e-05
|
|
|
MAPK9
|
[NCBI]
|
2.64163e-05
|
|
|
LTA
|
[NCBI]
|
2.55508e-05
|
|
|
EGF
|
[NCBI]
|
2.51415e-05
|
|
|
NPHS1
|
[NCBI]
|
2.51321e-05
|
|
|
LRS1
|
[NCBI]
|
2.36921e-05
|
|
|
AS
|
[NCBI]
|
2.36108e-05
|
|
|
ARSB
|
[NCBI]
|
2.31579e-05
|
|
|
CFB
|
[NCBI]
|
2.26015e-05
|
|
|
ABS
|
[NCBI]
|
2.23566e-05
|
|
|
APCS
|
[NCBI]
|
2.16065e-05
|
|
|
CTSC
|
[NCBI]
|
2.13785e-05
|
|
|
COL3A1
|
[NCBI]
|
2.07365e-05
|
|
|
EDN1
|
[NCBI]
|
1.9964e-05
|
|
|
HFTC
|
[NCBI]
|
1.99539e-05
|
|
|
MNS
|
[NCBI]
|
1.99539e-05
|
|
|
COL1A2
|
[NCBI]
|
1.86394e-05
|
|
|
TGFB1
|
[NCBI]
|
1.72804e-05
|
|
|
mucopolysaccharidosis type vii
|
[NCBI]
|
1.68948e-05
|
|
|
SOCS3
|
[NCBI]
|
1.61507e-05
|
|
|
STC1
|
[NCBI]
|
1.56505e-05
|
|
|
GUSB
|
[NCBI]
|
1.36714e-05
|
|
|
ACP5
|
[NCBI]
|
1.281e-05
|
|
|
FMF
|
[NCBI]
|
1.28026e-05
|
|
|
PLAUR
|
[NCBI]
|
1.27477e-05
|
|
|
TNFSF11
|
[NCBI]
|
1.2275e-05
|
|
|
SJS1
|
[NCBI]
|
1.21887e-05
|
|
|
UCN
|
[NCBI]
|
1.18357e-05
|
|
|
SLPI
|
[NCBI]
|
1.15763e-05
|
|
|
IL6
|
[NCBI]
|
1.15258e-05
|
|
|
BGLAP
|
[NCBI]
|
1.1183e-05
|
|
|
FAAH
|
[NCBI]
|
1.01775e-05
|
|
|
NGFB
|
[NCBI]
|
9.90994e-06
|
|
|
ABP1
|
[NCBI]
|
9.21667e-06
|
|
|
bullous erythroderma ichthyosiformis congenita of brocq
|
[NCBI]
|
8.76779e-06
|
|
|
CTGF
|
[NCBI]
|
3.37469e-06
|
|
|
PTHLH
|
[NCBI]
|
2.80543e-06
|
|
|
XDH
|
[NCBI]
|
2.4445e-06
|
|
|
VIP
|
[NCBI]
|
1.95414e-06
|
|
|
CRH
|
[NCBI]
|
1.7009e-06
|
|
|
BDNF
|
[NCBI]
|
1.3176e-06
|
|
|
SHH
|
[NCBI]
|
1.0454e-06
|
|
|
ADA
|
[NCBI]
|
7.83466e-07
|
|
|
MPO
|
[NCBI]
|
5.85554e-07
|
|
|
PTK2
|
[NCBI]
|
3.27556e-07
|
|
|
PCNA
|
[NCBI]
|
3.1405e-07
|
|
|
TH
|
[NCBI]
|
2.26115e-07
|
|
|
PTH
|
[NCBI]
|
1.77783e-07
|
|
|
NPY
|
[NCBI]
|
1.68764e-07
|
|
|
TNFSF6
|
[NCBI]
|
1.54844e-07
|
|