|
OMIM |
Link |
Information gain |
01 |
|
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency
|
[NCBI]
|
0.000292464
|
|
|
adrenal hyperplasia, congenital, due to steroid 11-beta-hydroxylase deficiency
|
[NCBI]
|
0.000290741
|
|
|
AMH
|
[NCBI]
|
0.000155404
|
|
|
hyperostosis frontalis interna
|
[NCBI]
|
0.000118925
|
|
|
AR
|
[NCBI]
|
0.00011179
|
|
|
AIS
|
[NCBI]
|
0.000106601
|
|
|
rokitansky-kuster-hauser syndrome
|
[NCBI]
|
9.25519e-05
|
|
|
CYP19A1
|
[NCBI]
|
9.02147e-05
|
|
|
BWS
|
[NCBI]
|
8.83413e-05
|
|
|
pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities
|
[NCBI]
|
8.5626e-05
|
|
|
diabetes mellitus, insulin-resistant, with acanthosis nigricans
|
[NCBI]
|
8.18742e-05
|
|
|
STAR
|
[NCBI]
|
7.47255e-05
|
|
|
hyperglycerolemia
|
[NCBI]
|
7.15296e-05
|
|
|
ABS
|
[NCBI]
|
7.03965e-05
|
|
|
WNT4
|
[NCBI]
|
5.89909e-05
|
|
|
BBS
|
[NCBI]
|
4.69181e-05
|
|
|
GK
|
[NCBI]
|
4.67012e-05
|
|
|
CYP11B1
|
[NCBI]
|
4.44269e-05
|
|
|
GCCR
|
[NCBI]
|
3.90767e-05
|
|
|
INSR
|
[NCBI]
|
2.78257e-05
|
|
|
von willebrand disease
|
[NCBI]
|
2.6298e-05
|
|
|
APC
|
[NCBI]
|
1.37366e-05
|
|
|
AFP
|
[NCBI]
|
1.25877e-05
|
|
|
SHBG
|
[NCBI]
|
1.12951e-05
|
|
|
VIP
|
[NCBI]
|
7.78256e-06
|
|
|
PRL
|
[NCBI]
|
1.14718e-06
|
|