|
OMIM |
Link |
Information gain |
01 |
|
AIS
|
[NCBI]
|
0.00157721
|
|
|
pseudohermaphroditism, female, with skeletal anomalies
|
[NCBI]
|
0.00137383
|
|
|
hermaphroditism, true
|
[NCBI]
|
0.00122708
|
|
|
trichoscyphodysplasia
|
[NCBI]
|
0.00115589
|
|
|
pseudohermaphroditism, incomplete male, type i
|
[NCBI]
|
0.000424736
|
|
|
SRA2
|
[NCBI]
|
0.000423313
|
|
|
SRY
|
[NCBI]
|
0.000359948
|
|
|
palmoplantar hyperkeratosis with squamous cell carcinoma of skin and sex reversal
|
[NCBI]
|
0.000174809
|
|
|
reifenstein syndrome
|
[NCBI]
|
0.000165434
|
|
|
17-@beta hydroxysteroid dehydrogenase iii deficiency
|
[NCBI]
|
0.000147287
|
|
|
GDXY
|
[NCBI]
|
0.000147211
|
|
|
denys-drash syndrome
|
[NCBI]
|
0.000145055
|
|
|
PPSH
|
[NCBI]
|
0.000121644
|
|
|
AMH
|
[NCBI]
|
0.000102966
|
|
|
myotubular myopathy with abnormal genital development
|
[NCBI]
|
9.02278e-05
|
|
|
hypogonadism, male
|
[NCBI]
|
8.47286e-05
|
|
|
gracile bone dysplasia
|
[NCBI]
|
7.73868e-05
|
|
|
AR
|
[NCBI]
|
7.66824e-05
|
|
|
GULP1
|
[NCBI]
|
6.86113e-05
|
|
|
B3GALT5
|
[NCBI]
|
6.86113e-05
|
|
|
FGF9
|
[NCBI]
|
6.34123e-05
|
|
|
lipoid congenital adrenal hyperplasia
|
[NCBI]
|
6.06627e-05
|
|
|
CXORF6
|
[NCBI]
|
6.0037e-05
|
|
|
SLOS
|
[NCBI]
|
5.97942e-05
|
|
|
adrenal hyperplasia, congenital, due to 17-alpha-hydroxylase deficiency
|
[NCBI]
|
5.69765e-05
|
|
|
HMCN1
|
[NCBI]
|
5.55285e-05
|
|
|
JBS
|
[NCBI]
|
5.39878e-05
|
|
|
ATRX
|
[NCBI]
|
5.09058e-05
|
|
|
ACTA1
|
[NCBI]
|
5.00962e-05
|
|
|
RAC1
|
[NCBI]
|
4.82005e-05
|
|
|
3-@beta-hydroxysteroid dehydrogenase, type ii, deficiency of
|
[NCBI]
|
4.66106e-05
|
|
|
spermatogenic failure, nonobstructive, y-linked
|
[NCBI]
|
4.53184e-05
|
|
|
FOXL2
|
[NCBI]
|
4.34898e-05
|
|
|
BPES
|
[NCBI]
|
4.03473e-05
|
|
|
MTM1
|
[NCBI]
|
4.03473e-05
|
|
|
NR5A1
|
[NCBI]
|
4.03164e-05
|
|
|
WT1
|
[NCBI]
|
3.30189e-05
|
|
|
WT1
|
[NCBI]
|
3.15959e-05
|
|
|
LRP1
|
[NCBI]
|
2.50329e-05
|
|
|
TP53
|
[NCBI]
|
1.9184e-05
|
|
|
SHBG
|
[NCBI]
|
1.00437e-05
|
|
|
EGF
|
[NCBI]
|
3.83853e-08
|
|