|
OMIM |
Link |
Information gain |
01 |
|
gonadal dysgenesis, xy type
|
[NCBI]
|
0.00576818
|
|
|
SRY
|
[NCBI]
|
0.00100299
|
|
|
GBY
|
[NCBI]
|
0.000673834
|
|
|
GCY
|
[NCBI]
|
0.000647644
|
|
|
OFD4
|
[NCBI]
|
0.000572697
|
|
|
GDXY
|
[NCBI]
|
0.000456489
|
|
|
TRS
|
[NCBI]
|
0.000300238
|
|
|
NR5A1
|
[NCBI]
|
0.000272412
|
|
|
agonadism with multiple internal malformations
|
[NCBI]
|
0.000230506
|
|
|
campomelic dysplasia
|
[NCBI]
|
0.000216883
|
|
|
gonadal agenesis
|
[NCBI]
|
0.000216521
|
|
|
gonadal dysgenesis, 46,xy, partial, with minifascicular neuropathy
|
[NCBI]
|
0.000216521
|
|
|
AR
|
[NCBI]
|
0.000136144
|
|
|
DMRT1
|
[NCBI]
|
0.00013137
|
|
|
agonadism, xy, with mental retardation, short stature, retarded bone age, and multiple extragenital malformations
|
[NCBI]
|
0.000130439
|
|
|
gonadal dysgenesis, xy type, with associated anomalies
|
[NCBI]
|
0.000130439
|
|
|
alopecia universalis congenita, xy gonadal dysgenesis, and laryngomalacia
|
[NCBI]
|
0.000130439
|
|
|
SRA2
|
[NCBI]
|
0.000107108
|
|
|
DHH
|
[NCBI]
|
0.000105211
|
|
|
WT1
|
[NCBI]
|
0.000103663
|
|
|
monosomy 9p syndrome
|
[NCBI]
|
9.39907e-05
|
|
|
jejunal atresia with microcephaly and ocular anomalies
|
[NCBI]
|
8.98999e-05
|
|
|
frasier syndrome
|
[NCBI]
|
8.66409e-05
|
|
|
AIS
|
[NCBI]
|
8.45573e-05
|
|
|
ODG1
|
[NCBI]
|
7.95864e-05
|
|
|
PRKY
|
[NCBI]
|
7.93609e-05
|
|
|
SLOS
|
[NCBI]
|
7.77183e-05
|
|
|
LHX9
|
[NCBI]
|
6.55835e-05
|
|
|
DMRT2
|
[NCBI]
|
6.55835e-05
|
|
|
PPSH
|
[NCBI]
|
5.84605e-05
|
|
|
MCOPS7
|
[NCBI]
|
5.79589e-05
|
|
|
charge syndrome
|
[NCBI]
|
5.56645e-05
|
|
|
AMH
|
[NCBI]
|
5.43534e-05
|
|
|
PHS
|
[NCBI]
|
5.3289e-05
|
|
|
NS1
|
[NCBI]
|
4.0481e-05
|
|
|
SRD5A2
|
[NCBI]
|
3.85443e-05
|
|
|
SOX9
|
[NCBI]
|
3.6566e-05
|
|
|
WT1
|
[NCBI]
|
3.00374e-05
|
|
|
STAR
|
[NCBI]
|
2.59471e-05
|
|
|
SHBG
|
[NCBI]
|
7.5693e-06
|
|