|
OMIM |
Link |
Information
gain |
01 |
|
|
prognathism, mandibular
|
[NCBI]
|
0.00529653
|
|
|
|
osteodysplasia, familial, anderson type
|
[NCBI]
|
0.000880362
|
|
|
|
SHFM2
|
[NCBI]
|
0.000647644
|
|
|
|
GO
|
[NCBI]
|
0.000605677
|
|
|
|
PCA
|
[NCBI]
|
0.000588308
|
|
|
|
SHFM3
|
[NCBI]
|
0.000493306
|
|
|
|
EEC1
|
[NCBI]
|
0.00038891
|
|
|
|
SHFM1
|
[NCBI]
|
0.000376213
|
|
|
|
AS
|
[NCBI]
|
0.000272864
|
|
|
|
MCOPS8
|
[NCBI]
|
0.000229097
|
|
|
|
SNX3
|
[NCBI]
|
0.000223417
|
|
|
|
CCD
|
[NCBI]
|
0.000202246
|
|
|
|
brachioskeletogenital syndrome
|
[NCBI]
|
0.000136591
|
|
|
|
mental retardation, obesity, mandibular prognathism, and eye and skin anomalies
|
[NCBI]
|
0.000136591
|
|
|
|
split-foot deformity with mandibulofacial dysostosis
|
[NCBI]
|
0.000105643
|
|
|
|
oroacral syndrome, verloes-koulischer type
|
[NCBI]
|
0.000100139
|
|
|
|
SHFM4
|
[NCBI]
|
9.27854e-05
|
|
|
|
ankyloblepharon-ectodermal defects-cleft lip/palate
|
[NCBI]
|
8.23042e-05
|
|
|
|
adult syndrome
|
[NCBI]
|
7.9483e-05
|
|
|
|
BWS
|
[NCBI]
|
7.87134e-05
|
|
|
|
gm1-gangliosidosis, type iii
|
[NCBI]
|
7.14886e-05
|
|
|
|
RIEG1
|
[NCBI]
|
6.67501e-05
|
|
|
|
EVC
|
[NCBI]
|
6.13333e-05
|
|
|
|
sotos syndrome
|
[NCBI]
|
5.54634e-05
|
|
|
|
fragile x mental retardation syndrome
|
[NCBI]
|
3.82276e-05
|
|
