|
OMIM |
Link |
Information
gain |
01 |
|
|
molar i reinclusion
|
[NCBI]
|
0.00146918
|
|
|
|
HFM
|
[NCBI]
|
0.00101875
|
|
|
|
osteodysplasia, familial, anderson type
|
[NCBI]
|
0.000776146
|
|
|
|
maxillonasal dysplasia, binder type
|
[NCBI]
|
0.000570168
|
|
|
|
prognathism, mandibular
|
[NCBI]
|
0.000570168
|
|
|
|
CMDR
|
[NCBI]
|
0.000544115
|
|
|
|
STHAG4
|
[NCBI]
|
0.000544115
|
|
|
|
apnea, obstructive sleep
|
[NCBI]
|
0.000315558
|
|
|
|
kabuki syndrome
|
[NCBI]
|
0.000225491
|
|
|
|
CPI
|
[NCBI]
|
0.000200659
|
|
|
|
CCD
|
[NCBI]
|
0.000178078
|
|
|
|
HSS
|
[NCBI]
|
0.00014668
|
|
|
|
brachioskeletogenital syndrome
|
[NCBI]
|
0.000128816
|
|
|
|
cleft palate, midfacial hypoplasia, triangular facies, and sensorineural hearing loss
|
[NCBI]
|
0.000128816
|
|
|
|
SRS
|
[NCBI]
|
0.000112367
|
|
|
|
amelogenesis imperfecta, hypoplastic, and openbite malocclusion, autosomal recessive
|
[NCBI]
|
9.78725e-05
|
|
|
|
larynx, congenital partial atresia of
|
[NCBI]
|
8.82795e-05
|
|
|
|
STL3
|
[NCBI]
|
8.50211e-05
|
|
|
|
STL2
|
[NCBI]
|
8.23123e-05
|
|
|
|
AIH2
|
[NCBI]
|
7.79682e-05
|
|
|
|
lenz-majewski hyperostotic dwarfism
|
[NCBI]
|
7.6169e-05
|
|
|
|
ENAM
|
[NCBI]
|
7.24206e-05
|
|
|
|
BOS1
|
[NCBI]
|
6.82623e-05
|
|
|
|
EYA1
|
[NCBI]
|
6.5769e-05
|
|
|
|
crouzon syndrome
|
[NCBI]
|
6.45623e-05
|
|
|
|
PITX2
|
[NCBI]
|
6.36001e-05
|
|
|
|
RIEG1
|
[NCBI]
|
5.90339e-05
|
|
|
|
RCDP1
|
[NCBI]
|
5.44947e-05
|
|
|
|
STL1
|
[NCBI]
|
5.36412e-05
|
|
|
|
COH1
|
[NCBI]
|
5.20614e-05
|
|
|
|
SJS1
|
[NCBI]
|
5.09726e-05
|
|
|
|
VWS
|
[NCBI]
|
4.61782e-05
|
|
|
|
AMC
|
[NCBI]
|
4.44702e-05
|
|
|
|
SLS
|
[NCBI]
|
4.19213e-05
|
|
|
|
SVAS
|
[NCBI]
|
4.15347e-05
|
|
|
|
GNRH1
|
[NCBI]
|
3.79296e-05
|
|
|
|
WBS
|
[NCBI]
|
2.79581e-05
|
|
|
|
MFS
|
[NCBI]
|
2.44218e-05
|
|
|
|
RA
|
[NCBI]
|
9.07728e-06
|
|
|
|
CF
|
[NCBI]
|
7.89891e-06
|
|
