|
OMIM |
Link |
Information gain |
01 |
|
HFM
|
[NCBI]
|
0.00864602
|
|
|
TCOF
|
[NCBI]
|
0.00672212
|
|
|
POADS
|
[NCBI]
|
0.00424368
|
|
|
maxillofacial dysostosis
|
[NCBI]
|
0.00185702
|
|
|
TCOF1
|
[NCBI]
|
0.00184408
|
|
|
acrodysostosis
|
[NCBI]
|
0.00111036
|
|
|
AFD1
|
[NCBI]
|
0.000640114
|
|
|
hemifacial microsomia with radial defects
|
[NCBI]
|
0.000533713
|
|
|
lateral meningocele syndrome
|
[NCBI]
|
0.000533713
|
|
|
branchial arch syndrome, x-linked
|
[NCBI]
|
0.000439076
|
|
|
acrofacial dysostosis syndrome of rodriguez
|
[NCBI]
|
0.000361638
|
|
|
mandibulofacial dysostosis, treacher collins type, autosomal recessive
|
[NCBI]
|
0.000329068
|
|
|
MNS
|
[NCBI]
|
0.000267154
|
|
|
HSS
|
[NCBI]
|
0.000264147
|
|
|
acrofacial dysostosis, catania type
|
[NCBI]
|
0.00021922
|
|
|
NDST1
|
[NCBI]
|
0.000208113
|
|
|
cataract, membranous
|
[NCBI]
|
0.000109532
|
|
|
mandibulofacial dysostosis syndrome, bauru type
|
[NCBI]
|
0.000109532
|
|
|
growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate
|
[NCBI]
|
0.000109532
|
|
|
mandibulofacial dysostosis with ptosis, autosomal dominant
|
[NCBI]
|
0.000109532
|
|
|
mandibulofacial dysostosis with macroblepharon and macrostomia
|
[NCBI]
|
0.000109532
|
|
|
lambert syndrome
|
[NCBI]
|
8.70777e-05
|
|
|
split-foot deformity with mandibulofacial dysostosis
|
[NCBI]
|
7.86143e-05
|
|
|
WS1
|
[NCBI]
|
7.76269e-05
|
|
|
robin sequence with cleft mandible and limb anomalies
|
[NCBI]
|
7.31247e-05
|
|
|
PRRX2
|
[NCBI]
|
7.10704e-05
|
|
|
CDX1
|
[NCBI]
|
7.10704e-05
|
|
|
TBL1X
|
[NCBI]
|
6.58708e-05
|
|
|
weyers acrofacial dysostosis
|
[NCBI]
|
6.58022e-05
|
|
|
aglossia-adactylia
|
[NCBI]
|
6.58022e-05
|
|
|
PITX1
|
[NCBI]
|
6.24949e-05
|
|
|
PMX1
|
[NCBI]
|
5.99851e-05
|
|
|
serpentine fibula-polycystic kidney syndrome
|
[NCBI]
|
5.87887e-05
|
|
|
EVC2
|
[NCBI]
|
5.63228e-05
|
|
|
DBA
|
[NCBI]
|
5.60192e-05
|
|
|
frank-ter haar syndrome
|
[NCBI]
|
5.48997e-05
|
|
|
CXORF5
|
[NCBI]
|
5.25509e-05
|
|
|
PDGFRB
|
[NCBI]
|
4.90631e-05
|
|
|
UBTF
|
[NCBI]
|
4.90631e-05
|
|
|
FMD
|
[NCBI]
|
4.72443e-05
|
|
|
pycnodysostosis
|
[NCBI]
|
4.72443e-05
|
|
|
crouzon syndrome
|
[NCBI]
|
4.55272e-05
|
|
|
PAFAH1B1
|
[NCBI]
|
4.49227e-05
|
|
|
MADA
|
[NCBI]
|
4.12904e-05
|
|
|
diastrophic dysplasia
|
[NCBI]
|
4.12904e-05
|
|
|
OFD1
|
[NCBI]
|
4.01038e-05
|
|
|
andersen cardiodysrhythmic periodic paralysis
|
[NCBI]
|
3.95435e-05
|
|
|
ODDD
|
[NCBI]
|
3.61144e-05
|
|
|
PAX3
|
[NCBI]
|
3.42405e-05
|
|
|
HGPS
|
[NCBI]
|
2.46328e-05
|
|
|
GJA1
|
[NCBI]
|
2.43228e-05
|
|
|
CD
|
[NCBI]
|
1.83717e-05
|
|
|
BCNS
|
[NCBI]
|
1.32133e-05
|
|