|
OMIM |
Link |
Information
gain |
01 |
|
|
striae distensae, familial
|
[NCBI]
|
0.00277021
|
|
|
|
adrenal unresponsiveness to acth
|
[NCBI]
|
0.0020498
|
|
|
|
hypoadrenocorticism, familial
|
[NCBI]
|
0.0020498
|
|
|
|
GCCD1
|
[NCBI]
|
0.000651804
|
|
|
|
corticosteroid-binding globulin deficiency
|
[NCBI]
|
0.000240309
|
|
|
|
lipoid congenital adrenal hyperplasia
|
[NCBI]
|
0.000211647
|
|
|
|
adrenal hyperplasia, congenital, due to 17-alpha-hydroxylase deficiency
|
[NCBI]
|
0.000200903
|
|
|
|
pituitary dwarfism with small sella turcica
|
[NCBI]
|
0.000174058
|
|
|
|
ataxia-deafness-retardation syndrome
|
[NCBI]
|
0.000174058
|
|
|
|
AIMAH
|
[NCBI]
|
0.000170699
|
|
|
|
GRA
|
[NCBI]
|
0.000149659
|
|
|
|
gynecomastia, familial
|
[NCBI]
|
0.000142478
|
|
|
|
ichthyosis and male hypogonadism
|
[NCBI]
|
0.000142478
|
|
|
|
pseudohermaphroditism, incomplete male, type i
|
[NCBI]
|
0.000130565
|
|
|
|
BJS
|
[NCBI]
|
0.000130565
|
|
|
|
AME2
|
[NCBI]
|
0.000122832
|
|
|
|
PPNAD1
|
[NCBI]
|
0.000117085
|
|
|
|
corticosterone methyloxidase type i deficiency
|
[NCBI]
|
0.000112507
|
|
|
|
por deficiency
|
[NCBI]
|
0.000100075
|
|
|
|
ALMS
|
[NCBI]
|
9.7803e-05
|
|
|
|
CNC1
|
[NCBI]
|
8.89772e-05
|
|
|
|
AAA
|
[NCBI]
|
8.26583e-05
|
|
|
|
adrenal hyperplasia, congenital, due to steroid 11-beta-hydroxylase deficiency
|
[NCBI]
|
8.26583e-05
|
|
|
|
sotos syndrome
|
[NCBI]
|
8.05582e-05
|
|
|
|
RA
|
[NCBI]
|
7.23571e-05
|
|
|
|
GDXY
|
[NCBI]
|
6.59573e-05
|
|
|
|
CRH
|
[NCBI]
|
4.48275e-05
|
|
|
|
SERPINA6
|
[NCBI]
|
4.06669e-05
|
|
|
|
POR
|
[NCBI]
|
3.43407e-05
|
|
|
|
CYP11B2
|
[NCBI]
|
2.79758e-05
|
|
|
|
KAL1
|
[NCBI]
|
2.72525e-05
|
|
|
|
ALD
|
[NCBI]
|
2.57136e-05
|
|
|
|
GCCR
|
[NCBI]
|
2.41595e-05
|
|
|
|
cortisol 11-beta-ketoreductase deficiency
|
[NCBI]
|
2.30077e-05
|
|
|
|
PWS
|
[NCBI]
|
2.07448e-05
|
|
|
|
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency
|
[NCBI]
|
1.86277e-05
|
|
|
|
AVP
|
[NCBI]
|
1.34801e-05
|
|
