|
OMIM |
Link |
Information gain |
01 |
|
BGS
|
[NCBI]
|
0.00201402
|
|
|
FGFR2
|
[NCBI]
|
0.00198725
|
|
|
CRSA
|
[NCBI]
|
0.00197839
|
|
|
cdags syndrome
|
[NCBI]
|
0.00197839
|
|
|
ABS
|
[NCBI]
|
0.00176673
|
|
|
CFNS
|
[NCBI]
|
0.00133548
|
|
|
hypertelorism, teebi type
|
[NCBI]
|
0.00132132
|
|
|
cranioectodermal dysplasia
|
[NCBI]
|
0.00127273
|
|
|
FGFR3
|
[NCBI]
|
0.00123837
|
|
|
JWS
|
[NCBI]
|
0.000924043
|
|
|
CRS1
|
[NCBI]
|
0.000864599
|
|
|
SCS
|
[NCBI]
|
0.000835993
|
|
|
hypomandibular faciocranial dysostosis
|
[NCBI]
|
0.000766909
|
|
|
muenke syndrome
|
[NCBI]
|
0.000701009
|
|
|
sprengel deformity
|
[NCBI]
|
0.000684933
|
|
|
shprintzen-goldberg craniosynostosis syndrome
|
[NCBI]
|
0.000677681
|
|
|
MCOPS4
|
[NCBI]
|
0.0006318
|
|
|
SGM1
|
[NCBI]
|
0.0006318
|
|
|
prognathism, mandibular
|
[NCBI]
|
0.000561
|
|
|
acromelic frontonasal dysostosis
|
[NCBI]
|
0.000561
|
|
|
OSCS
|
[NCBI]
|
0.000561
|
|
|
MCOPS6
|
[NCBI]
|
0.000534964
|
|
|
c syndrome
|
[NCBI]
|
0.000516332
|
|
|
hennekam lymphangiectasia-lymphedema syndrome
|
[NCBI]
|
0.000512719
|
|
|
pfeiffer syndrome
|
[NCBI]
|
0.000486722
|
|
|
ear, patella, short stature syndrome
|
[NCBI]
|
0.000476092
|
|
|
MCOP1
|
[NCBI]
|
0.000476092
|
|
|
MCOPS1
|
[NCBI]
|
0.000460635
|
|
|
trigonocephaly, nonsyndromic
|
[NCBI]
|
0.000390421
|
|
|
craniostenosis, sagittal, with congenital heart disease, mental deficiency, and mandibular ankylosis
|
[NCBI]
|
0.000390421
|
|
|
por deficiency
|
[NCBI]
|
0.000376045
|
|
|
MSX2
|
[NCBI]
|
0.00036325
|
|
|
dubowitz syndrome
|
[NCBI]
|
0.000337721
|
|
|
carpenter syndrome
|
[NCBI]
|
0.000313045
|
|
|
crouzon syndrome
|
[NCBI]
|
0.000306481
|
|
|
TWIST1
|
[NCBI]
|
0.000299064
|
|
|
furlong syndrome: fs
|
[NCBI]
|
0.000256279
|
|
|
craniosynostosis with ectopia lentis
|
[NCBI]
|
0.000256279
|
|
|
CRS2
|
[NCBI]
|
0.000256279
|
|
|
apert syndrome
|
[NCBI]
|
0.00025192
|
|
|
hunter-mcalpine craniosynostosis syndrome
|
[NCBI]
|
0.000238232
|
|
|
POR
|
[NCBI]
|
0.00022508
|
|
|
FGFR1
|
[NCBI]
|
0.000222732
|
|
|
trigonocephaly with short stature and developmental delay
|
[NCBI]
|
0.000195061
|
|
|
craniosynostosis-mental retardation syndrome of lin and gettig
|
[NCBI]
|
0.000195061
|
|
|
craniomicromelic syndrome
|
[NCBI]
|
0.000195061
|
|
|
kleeblattschaedel syndrome
|
[NCBI]
|
0.000195061
|
|
|
craniosynostosis with fibular aplasia
|
[NCBI]
|
0.000195061
|
|
|
lowry-maclean syndrome
|
[NCBI]
|
0.000164145
|
|
|
bone fragility with craniosynostosis, ocular proptosis, hydrocephalus, and distinctive facial features
|
[NCBI]
|
0.000164145
|
|
|
EFNB1
|
[NCBI]
|
0.000161891
|
|
|
oculopalatoskeletal syndrome
|
[NCBI]
|
0.000150194
|
|
|
cutis gyrata syndrome of beare and stevenson
|
[NCBI]
|
0.000140629
|
|
|
ruvalcaba syndrome
|
[NCBI]
|
0.000127369
|
|
|
SNAI1
|
[NCBI]
|
0.000107822
|
|
|
LDS
|
[NCBI]
|
0.000105019
|
|
|
craniosynostosis with anomalies of the cranial base and digits
|
[NCBI]
|
9.74931e-05
|
|
|
craniosynostosis with ocular abnormalities and hallucal defects
|
[NCBI]
|
9.74931e-05
|
|
|
craniosynostosis, calcification of basal ganglia, and facial dysmorphism
|
[NCBI]
|
9.74931e-05
|
|
|
aurocephalosyndactyly
|
[NCBI]
|
9.74931e-05
|
|
|
craniosynostosis
|
[NCBI]
|
9.74931e-05
|
|
|
craniosynostosis-mental retardation-clefting syndrome
|
[NCBI]
|
9.74931e-05
|
|
|
scaphocephaly, maxillary retrusion, and mental retardation
|
[NCBI]
|
9.74931e-05
|
|
|
craniosynostosis, sagittal, with dandy-walker malformation and hydrocephalus
|
[NCBI]
|
9.74931e-05
|
|
|
lambdoid synostosis
|
[NCBI]
|
9.74931e-05
|
|
|
craniosynostosis, philadelphia type
|
[NCBI]
|
9.74931e-05
|
|
|
spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and mental retardation
|
[NCBI]
|
9.74931e-05
|
|
|
craniosynostosis syndrome, autosomal recessive
|
[NCBI]
|
9.74931e-05
|
|
|
holoprosencephaly, semilobar, with craniosynostosis
|
[NCBI]
|
9.74931e-05
|
|
|
acrocephalopolysyndactyly type iii
|
[NCBI]
|
9.74931e-05
|
|
|
acrocraniofacial dysostosis
|
[NCBI]
|
9.74931e-05
|
|
|
JBS
|
[NCBI]
|
9.20892e-05
|
|
|
frontoocular syndrome
|
[NCBI]
|
7.506e-05
|
|
|
summitt syndrome
|
[NCBI]
|
7.506e-05
|
|
|
craniorhiny
|
[NCBI]
|
7.506e-05
|
|
|
holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate
|
[NCBI]
|
7.506e-05
|
|
|
craniosynostosis-microcephaly with chromosomal breakage and other abnormalities
|
[NCBI]
|
7.506e-05
|
|
|
MCOP3
|
[NCBI]
|
6.66174e-05
|
|
|
acrocephalopolydactylous dysplasia
|
[NCBI]
|
6.66174e-05
|
|
|
craniofacial dyssynostosis with short stature
|
[NCBI]
|
6.66174e-05
|
|
|
MCOPS5
|
[NCBI]
|
6.66174e-05
|
|
|
craniotelencephalic dysplasia
|
[NCBI]
|
6.66174e-05
|
|
|
carnevale syndrome
|
[NCBI]
|
6.66174e-05
|
|
|
GCPS
|
[NCBI]
|
6.41212e-05
|
|
|
microcephaly with chemotactic defect and transient hypogammaglobulinemia
|
[NCBI]
|
6.11486e-05
|
|
|
P4HA3
|
[NCBI]
|
5.9054e-05
|
|
|
TWISTNB
|
[NCBI]
|
5.9054e-05
|
|
|
apnea, obstructive sleep
|
[NCBI]
|
5.83437e-05
|
|
|
MCOP2
|
[NCBI]
|
5.70922e-05
|
|
|
robinow-sorauf syndrome
|
[NCBI]
|
5.70922e-05
|
|
|
mental retardation, fra12a type
|
[NCBI]
|
5.38677e-05
|
|
|
cerebellotrigeminal dermal dysplasia
|
[NCBI]
|
5.38677e-05
|
|
|
SOX6
|
[NCBI]
|
5.3859e-05
|
|
|
TD2
|
[NCBI]
|
4.89087e-05
|
|
|
frontonasal dysplasia
|
[NCBI]
|
4.89087e-05
|
|
|
MFS2
|
[NCBI]
|
4.69167e-05
|
|
|
OGD
|
[NCBI]
|
4.69167e-05
|
|
|
lenz-majewski hyperostotic dwarfism
|
[NCBI]
|
4.51513e-05
|
|
|
cherubism
|
[NCBI]
|
4.51513e-05
|
|
|
MCOPS9
|
[NCBI]
|
4.35672e-05
|
|
|
sc phocomelia syndrome
|
[NCBI]
|
4.35672e-05
|
|
|
wildervanck syndrome
|
[NCBI]
|
4.2131e-05
|
|
|
RECQL4
|
[NCBI]
|
4.16715e-05
|
|
|
MCOPS2
|
[NCBI]
|
3.96095e-05
|
|
|
TCF3
|
[NCBI]
|
3.9582e-05
|
|
|
MFS
|
[NCBI]
|
3.86604e-05
|
|
|
BDC
|
[NCBI]
|
3.84902e-05
|
|
|
PFM
|
[NCBI]
|
3.84902e-05
|
|
|
MCOPS3
|
[NCBI]
|
3.6474e-05
|
|
|
FMD
|
[NCBI]
|
3.55595e-05
|
|
|
GLDC
|
[NCBI]
|
3.40012e-05
|
|
|
NOG
|
[NCBI]
|
3.29935e-05
|
|
|
hyperimmunoglobulin e recurrent infection syndrome, autosomal dominant
|
[NCBI]
|
2.9188e-05
|
|
|
FGF8
|
[NCBI]
|
2.81955e-05
|
|
|
MCOPS7
|
[NCBI]
|
2.61167e-05
|
|
|
HCH
|
[NCBI]
|
2.52277e-05
|
|
|
FGF2
|
[NCBI]
|
2.40376e-05
|
|
|
FDH
|
[NCBI]
|
2.14974e-05
|
|
|
IHH
|
[NCBI]
|
2.10395e-05
|
|
|
RTS
|
[NCBI]
|
1.8352e-05
|
|
|
sotos syndrome
|
[NCBI]
|
1.8352e-05
|
|
|
FBN1
|
[NCBI]
|
1.70012e-05
|
|
|
TCOF
|
[NCBI]
|
1.58563e-05
|
|
|
ALGS1
|
[NCBI]
|
1.52599e-05
|
|
|
TD1
|
[NCBI]
|
1.36423e-05
|
|
|
EGF
|
[NCBI]
|
8.00426e-06
|
|
|
SHH
|
[NCBI]
|
7.42315e-06
|
|
|
ACP5
|
[NCBI]
|
6.18531e-06
|
|
|
DGS
|
[NCBI]
|
4.13733e-06
|
|
|
CPI
|
[NCBI]
|
3.19539e-06
|
|
|
FA
|
[NCBI]
|
1.7638e-06
|
|
|
AVP
|
[NCBI]
|
1.12288e-07
|
|