|
OMIM |
Link |
Information gain |
01 |
|
SLE
|
[NCBI]
|
0.00313448
|
|
|
gapo syndrome
|
[NCBI]
|
0.00138193
|
|
|
stiff skin syndrome
|
[NCBI]
|
0.00130285
|
|
|
joint laxity, familial
|
[NCBI]
|
0.000819746
|
|
|
camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormal palmar creases
|
[NCBI]
|
0.000587372
|
|
|
AKE
|
[NCBI]
|
0.000545541
|
|
|
ehlers-danlos syndrome, type vib
|
[NCBI]
|
0.000512699
|
|
|
EPS
|
[NCBI]
|
0.000509599
|
|
|
STL1
|
[NCBI]
|
0.000495753
|
|
|
skin creases, multiple benign ring-shaped, of limbs
|
[NCBI]
|
0.000485681
|
|
|
ACG1A
|
[NCBI]
|
0.000462747
|
|
|
RA
|
[NCBI]
|
0.000401861
|
|
|
MVP
|
[NCBI]
|
0.00033954
|
|
|
FBN1
|
[NCBI]
|
0.000296174
|
|
|
CF
|
[NCBI]
|
0.000287174
|
|
|
proteus syndrome
|
[NCBI]
|
0.00028611
|
|
|
OFC1
|
[NCBI]
|
0.00026551
|
|
|
COL2A1
|
[NCBI]
|
0.000265178
|
|
|
MFS
|
[NCBI]
|
0.00018037
|
|
|
buschke-ollendorff syndrome
|
[NCBI]
|
0.000141926
|
|
|
contractural arachnodactyly, congenital
|
[NCBI]
|
0.000132949
|
|
|
STL2
|
[NCBI]
|
0.000117704
|
|
|
MFS2
|
[NCBI]
|
0.000108417
|
|
|
COL11A1
|
[NCBI]
|
0.000100331
|
|
|
ATS
|
[NCBI]
|
9.54368e-05
|
|
|
harrod syndrome
|
[NCBI]
|
9.26351e-05
|
|
|
hydrocephalus, tall stature, joint laxity, and kyphoscoliosis
|
[NCBI]
|
9.26351e-05
|
|
|
osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones, but without fractures
|
[NCBI]
|
9.26351e-05
|
|
|
ehlers-danlos syndrome, autosomal dominant, type unspecified
|
[NCBI]
|
9.26351e-05
|
|
|
OPPG
|
[NCBI]
|
8.63064e-05
|
|
|
SNRPB2
|
[NCBI]
|
7.85884e-05
|
|
|
POP1
|
[NCBI]
|
7.85884e-05
|
|
|
PPAC
|
[NCBI]
|
7.62916e-05
|
|
|
UCMD
|
[NCBI]
|
7.49027e-05
|
|
|
ELN
|
[NCBI]
|
7.0404e-05
|
|
|
epiphyseal dysplasia, multiple, with myopia and conductive deafness
|
[NCBI]
|
7.02159e-05
|
|
|
EXOSC10
|
[NCBI]
|
6.48113e-05
|
|
|
TNR
|
[NCBI]
|
6.48113e-05
|
|
|
mass syndrome
|
[NCBI]
|
6.17872e-05
|
|
|
hyperimmunoglobulin g1(a1) syndrome
|
[NCBI]
|
6.17872e-05
|
|
|
heterotopia, periventricular, ehlers-danlos variant
|
[NCBI]
|
5.63323e-05
|
|
|
acrogeria, gottron type
|
[NCBI]
|
5.63323e-05
|
|
|
SLC2A10
|
[NCBI]
|
5.62393e-05
|
|
|
PXE
|
[NCBI]
|
5.58424e-05
|
|
|
COL5A2
|
[NCBI]
|
5.37312e-05
|
|
|
CENPC1
|
[NCBI]
|
5.37312e-05
|
|
|
WISP3
|
[NCBI]
|
5.17332e-05
|
|
|
stickler syndrome, type i, nonsyndromic ocular
|
[NCBI]
|
4.90792e-05
|
|
|
STL3
|
[NCBI]
|
4.90792e-05
|
|
|
MMP14
|
[NCBI]
|
4.63055e-05
|
|
|
TNXB
|
[NCBI]
|
4.44121e-05
|
|
|
COL6A2
|
[NCBI]
|
4.44121e-05
|
|
|
COL11A2
|
[NCBI]
|
4.28246e-05
|
|
|
HGD
|
[NCBI]
|
4.28246e-05
|
|
|
PCNA
|
[NCBI]
|
4.25743e-05
|
|
|
AOII
|
[NCBI]
|
4.21698e-05
|
|
|
weill-marchesani syndrome, autosomal recessive
|
[NCBI]
|
4.04183e-05
|
|
|
FN1
|
[NCBI]
|
4.02585e-05
|
|
|
noonan-like/multiple giant cell lesion syndrome
|
[NCBI]
|
3.8848e-05
|
|
|
shprintzen-goldberg craniosynostosis syndrome
|
[NCBI]
|
3.8848e-05
|
|
|
PEPD
|
[NCBI]
|
3.86961e-05
|
|
|
TNFSF13B
|
[NCBI]
|
3.86961e-05
|
|
|
antiphospholipid syndrome
|
[NCBI]
|
3.74258e-05
|
|
|
WSS
|
[NCBI]
|
3.74258e-05
|
|
|
COL6A1
|
[NCBI]
|
3.73491e-05
|
|
|
TGFBR2
|
[NCBI]
|
3.65444e-05
|
|
|
WZS
|
[NCBI]
|
3.61268e-05
|
|
|
LDS
|
[NCBI]
|
3.61268e-05
|
|
|
complement component 2 deficiency
|
[NCBI]
|
3.58009e-05
|
|
|
GLB1
|
[NCBI]
|
3.38607e-05
|
|
|
kniest dysplasia
|
[NCBI]
|
3.38266e-05
|
|
|
WGN1
|
[NCBI]
|
3.38266e-05
|
|
|
LOX
|
[NCBI]
|
3.30189e-05
|
|
|
FLNA
|
[NCBI]
|
3.30189e-05
|
|
|
cutis laxa, autosomal recessive, type ii
|
[NCBI]
|
3.27986e-05
|
|
|
mucopolysaccharidosis type iva
|
[NCBI]
|
2.94634e-05
|
|
|
cutis laxa, autosomal recessive, type i
|
[NCBI]
|
2.85325e-05
|
|
|
GABEB
|
[NCBI]
|
2.71301e-05
|
|
|
cutis laxa, x-linked
|
[NCBI]
|
2.58564e-05
|
|
|
alkaptonuria
|
[NCBI]
|
2.36184e-05
|
|
|
ehlers-danlos syndrome, type i
|
[NCBI]
|
1.96506e-05
|
|
|
COH1
|
[NCBI]
|
1.78889e-05
|
|
|
ACE
|
[NCBI]
|
1.37944e-05
|
|
|
HGPS
|
[NCBI]
|
1.03388e-05
|
|
|
SVAS
|
[NCBI]
|
9.27604e-06
|
|
|
osteogenesis imperfecta, type i
|
[NCBI]
|
8.99475e-06
|
|
|
MG
|
[NCBI]
|
8.56853e-06
|
|
|
VEGF
|
[NCBI]
|
8.34409e-06
|
|
|
SPP1
|
[NCBI]
|
7.05443e-06
|
|
|
MPO
|
[NCBI]
|
5.82792e-06
|
|
|
FMF
|
[NCBI]
|
5.66492e-06
|
|
|
polycystic kidneys
|
[NCBI]
|
2.92958e-06
|
|
|
CAT
|
[NCBI]
|
2.78825e-06
|
|
|
WBS
|
[NCBI]
|
1.2541e-06
|
|
|
PTH
|
[NCBI]
|
7.47815e-07
|
|
|
EGFR
|
[NCBI]
|
2.76372e-07
|
|
|
CD
|
[NCBI]
|
1.84692e-07
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
3.8771e-10
|
|
|
PRL
|
[NCBI]
|
2.90647e-10
|
|