|
OMIM |
Link |
Information gain |
01 |
|
HFM
|
[NCBI]
|
0.0320016
|
|
|
cayler cardiofacial syndrome
|
[NCBI]
|
0.00319695
|
|
|
hemifacial microsomia with radial defects
|
[NCBI]
|
0.00175016
|
|
|
proteus syndrome
|
[NCBI]
|
0.000577283
|
|
|
HFH
|
[NCBI]
|
0.000540115
|
|
|
HFA
|
[NCBI]
|
0.00040697
|
|
|
oculodentoosseous dysplasia, recessive
|
[NCBI]
|
0.00040697
|
|
|
microtia-anotia
|
[NCBI]
|
0.000368517
|
|
|
dysgnathia complex
|
[NCBI]
|
0.000368517
|
|
|
auriculocondylar syndrome
|
[NCBI]
|
0.000368517
|
|
|
rokitansky-kuster-hauser syndrome
|
[NCBI]
|
0.000314952
|
|
|
camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormal palmar creases
|
[NCBI]
|
0.00031308
|
|
|
hairy elbows
|
[NCBI]
|
0.000291817
|
|
|
HTC1
|
[NCBI]
|
0.000273386
|
|
|
microtia with meatal atresia and conductive deafness
|
[NCBI]
|
0.000273386
|
|
|
hemifacial myohyperplasia
|
[NCBI]
|
0.000266456
|
|
|
kenny-caffey syndrome, type 2
|
[NCBI]
|
0.000242681
|
|
|
dandy-walker-like malformation with atrioventricular septal defect
|
[NCBI]
|
0.000156788
|
|
|
DA2A
|
[NCBI]
|
0.000142322
|
|
|
TBS
|
[NCBI]
|
0.000140477
|
|
|
deafness-craniofacial syndrome
|
[NCBI]
|
0.00013289
|
|
|
speech development, delayed, with facial asymmetry, strabismus, and transverse earlobe crease
|
[NCBI]
|
0.00013289
|
|
|
facial asymmetry
|
[NCBI]
|
0.00013289
|
|
|
stratton-parker syndrome
|
[NCBI]
|
0.000110422
|
|
|
contractures, congenital, torticollis, and malignant hyperthermia
|
[NCBI]
|
0.000110422
|
|
|
MBS
|
[NCBI]
|
9.30604e-05
|
|
|
mental retardation, x-linked, with cerebellar hypoplasia and distinctive facial appearance
|
[NCBI]
|
9.23488e-05
|
|
|
poland syndrome
|
[NCBI]
|
8.9573e-05
|
|
|
hyperpipecolatemia
|
[NCBI]
|
8.40597e-05
|
|
|
PFN1
|
[NCBI]
|
7.46818e-05
|
|
|
CHD7
|
[NCBI]
|
7.26806e-05
|
|
|
HSR
|
[NCBI]
|
7.10164e-05
|
|
|
OPHN1
|
[NCBI]
|
6.83464e-05
|
|
|
AFD1
|
[NCBI]
|
6.63054e-05
|
|
|
SALL1
|
[NCBI]
|
6.53402e-05
|
|
|
SCDO1
|
[NCBI]
|
6.03874e-05
|
|
|
ODDD
|
[NCBI]
|
5.89692e-05
|
|
|
charge syndrome
|
[NCBI]
|
5.80894e-05
|
|
|
TCOF
|
[NCBI]
|
4.89295e-05
|
|
|
velocardiofacial syndrome
|
[NCBI]
|
4.82273e-05
|
|
|
ALGS1
|
[NCBI]
|
4.82273e-05
|
|
|
CDLS1
|
[NCBI]
|
4.00591e-05
|
|
|
FGFR3
|
[NCBI]
|
3.57117e-05
|
|
|
fragile x mental retardation syndrome
|
[NCBI]
|
3.46763e-05
|
|
|
klippel-trenaunay-weber syndrome
|
[NCBI]
|
1.64155e-05
|
|
|
PTH
|
[NCBI]
|
9.14044e-06
|
|
|
SRS
|
[NCBI]
|
3.72495e-08
|
|