|
OMIM |
Link |
Information gain |
01 |
|
hypertelorism with esophageal abnormality and hypospadias
|
[NCBI]
|
0.0219223
|
|
|
ocular hypotelorism, submucosal cleft palate, and hypospadias
|
[NCBI]
|
0.0017337
|
|
|
hypospadias, autosomal
|
[NCBI]
|
0.000906496
|
|
|
opitz syndrome
|
[NCBI]
|
0.000452782
|
|
|
AR
|
[NCBI]
|
0.00043469
|
|
|
AIS
|
[NCBI]
|
0.000379862
|
|
|
THAS
|
[NCBI]
|
0.000359343
|
|
|
SLOS
|
[NCBI]
|
0.000351831
|
|
|
reifenstein syndrome
|
[NCBI]
|
0.000351517
|
|
|
MCOPS1
|
[NCBI]
|
0.00034423
|
|
|
PPSH
|
[NCBI]
|
0.000340649
|
|
|
hypospadias, x-linked
|
[NCBI]
|
0.00033846
|
|
|
hand-foot-uterus syndrome
|
[NCBI]
|
0.00031604
|
|
|
schinzel-giedion midface-retraction syndrome
|
[NCBI]
|
0.000276949
|
|
|
robinow syndrome, autosomal dominant
|
[NCBI]
|
0.000260229
|
|
|
gastrointestinal abnormalities, multiple
|
[NCBI]
|
0.000194508
|
|
|
acrofrontofacionasal dysostosis, severe
|
[NCBI]
|
0.000194508
|
|
|
HOXA13
|
[NCBI]
|
0.000181532
|
|
|
charge-like syndrome, x-linked
|
[NCBI]
|
0.000180533
|
|
|
pseudohermaphroditism, incomplete male, type i
|
[NCBI]
|
0.0001636
|
|
|
ATF3
|
[NCBI]
|
0.000147679
|
|
|
urogenital adysplasia, hereditary
|
[NCBI]
|
0.000138788
|
|
|
CXORF6
|
[NCBI]
|
0.000135907
|
|
|
MID1
|
[NCBI]
|
0.000118759
|
|
|
kabuki syndrome
|
[NCBI]
|
0.000115576
|
|
|
hypertelorism and tetralogy of fallot
|
[NCBI]
|
0.000112629
|
|
|
brachioskeletogenital syndrome
|
[NCBI]
|
0.000112629
|
|
|
nasal bones, absence of
|
[NCBI]
|
0.000112629
|
|
|
acrorenal syndrome
|
[NCBI]
|
0.000112629
|
|
|
radial hypoplasia, triphalangeal thumbs, hypospadias, and maxillary diastema
|
[NCBI]
|
0.000112629
|
|
|
cryptomicrotia-brachydactyly syndrome
|
[NCBI]
|
0.000112629
|
|
|
wolff mental retardation syndrome
|
[NCBI]
|
0.000112629
|
|
|
hypospadias, hypertelorism, upper lid coloboma, and mixed-type hearing loss
|
[NCBI]
|
0.000112629
|
|
|
3-@beta-hydroxysteroid dehydrogenase, type ii, deficiency of
|
[NCBI]
|
0.000106419
|
|
|
MKKS
|
[NCBI]
|
0.000105678
|
|
|
charge syndrome
|
[NCBI]
|
9.89842e-05
|
|
|
SCS
|
[NCBI]
|
9.34726e-05
|
|
|
radial aplasia, x-linked
|
[NCBI]
|
9.01715e-05
|
|
|
stratton-parker syndrome
|
[NCBI]
|
9.01715e-05
|
|
|
infertile male syndrome
|
[NCBI]
|
8.17048e-05
|
|
|
myotubular myopathy with abnormal genital development
|
[NCBI]
|
8.17048e-05
|
|
|
GUD
|
[NCBI]
|
8.17048e-05
|
|
|
gynecomastia, familial
|
[NCBI]
|
8.17048e-05
|
|
|
preaxial deficiency, postaxial polydactyly, and hypospadias
|
[NCBI]
|
8.17048e-05
|
|
|
TAOK1
|
[NCBI]
|
8.16043e-05
|
|
|
GATA5
|
[NCBI]
|
8.16043e-05
|
|
|
anal atresia, hypospadias, and penoscrotal inversion
|
[NCBI]
|
7.6212e-05
|
|
|
cleft larynx, posterior
|
[NCBI]
|
6.88829e-05
|
|
|
WT1
|
[NCBI]
|
6.86527e-05
|
|
|
ZS
|
[NCBI]
|
6.23624e-05
|
|
|
HBQ1
|
[NCBI]
|
5.92523e-05
|
|
|
AMH
|
[NCBI]
|
5.87936e-05
|
|
|
wagr syndrome
|
[NCBI]
|
5.70017e-05
|
|
|
disorganization, mouse, homolog of
|
[NCBI]
|
5.56647e-05
|
|
|
alpha-thalassemia/mental retardation syndrome, deletion-type
|
[NCBI]
|
5.22226e-05
|
|
|
nondisjunction
|
[NCBI]
|
5.22226e-05
|
|
|
denys-drash syndrome
|
[NCBI]
|
5.22226e-05
|
|
|
MCOPS3
|
[NCBI]
|
5.12243e-05
|
|
|
KFSD
|
[NCBI]
|
4.94001e-05
|
|
|
RHS
|
[NCBI]
|
4.77666e-05
|
|
|
MADA
|
[NCBI]
|
4.43055e-05
|
|
|
RIEG1
|
[NCBI]
|
4.31123e-05
|
|
|
SRD5A2
|
[NCBI]
|
4.07727e-05
|
|
|
PKS
|
[NCBI]
|
4.04815e-05
|
|
|
MCOPS7
|
[NCBI]
|
4.04815e-05
|
|
|
ODDD
|
[NCBI]
|
3.90966e-05
|
|
|
ARX
|
[NCBI]
|
3.84385e-05
|
|
|
PHS
|
[NCBI]
|
3.5926e-05
|
|
|
ESD
|
[NCBI]
|
3.54753e-05
|
|
|
CMTC
|
[NCBI]
|
3.52282e-05
|
|
|
SRY
|
[NCBI]
|
3.01169e-05
|
|
|
LSA
|
[NCBI]
|
2.89525e-05
|
|
|
SRS
|
[NCBI]
|
2.83267e-05
|
|
|
HBA1
|
[NCBI]
|
2.33683e-05
|
|
|
FGFR2
|
[NCBI]
|
2.32968e-05
|
|
|
GJA1
|
[NCBI]
|
2.12039e-05
|
|
|
SHH
|
[NCBI]
|
1.49391e-05
|
|
|
EGF
|
[NCBI]
|
1.44181e-07
|
|