|
OMIM |
Link |
Information gain |
01 |
|
PCOS1
|
[NCBI]
|
0.00690869
|
|
|
SHBG
|
[NCBI]
|
0.00199536
|
|
|
dyssegmental dysplasia, rolland-desbuquois type
|
[NCBI]
|
0.00129172
|
|
|
cerebellar hypoplasia, mental retardation, and quadrupedal locomotion
|
[NCBI]
|
0.000694153
|
|
|
hypertrichosis universalis
|
[NCBI]
|
0.000570168
|
|
|
skin creases, multiple benign ring-shaped, of limbs
|
[NCBI]
|
0.000442837
|
|
|
schinzel-giedion midface-retraction syndrome
|
[NCBI]
|
0.000400267
|
|
|
coffin-siris syndrome
|
[NCBI]
|
0.000328512
|
|
|
hirsutism--skeletal dysplasia--mental retardation syndrome
|
[NCBI]
|
0.000274036
|
|
|
17-@beta hydroxysteroid dehydrogenase iii deficiency
|
[NCBI]
|
0.000178596
|
|
|
diabetes mellitus, insulin-resistant, with acanthosis nigricans
|
[NCBI]
|
0.000178596
|
|
|
PRL
|
[NCBI]
|
0.000169231
|
|
|
cyprus facial neuromusculoskeletal syndrome
|
[NCBI]
|
0.000136591
|
|
|
hypersecretion of adrenal androgens, familial
|
[NCBI]
|
0.000136591
|
|
|
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency
|
[NCBI]
|
0.000132213
|
|
|
alopecia, androgenetic
|
[NCBI]
|
0.000118136
|
|
|
fibromatosis, gingival, with hypertrichosis and mental retardation
|
[NCBI]
|
0.000114122
|
|
|
CDLS1
|
[NCBI]
|
0.000110348
|
|
|
CYP11A1
|
[NCBI]
|
0.000103546
|
|
|
barber-say syndrome
|
[NCBI]
|
9.6046e-05
|
|
|
cortisone reductase deficiency
|
[NCBI]
|
9.6046e-05
|
|
|
floating-harbor syndrome
|
[NCBI]
|
8.39246e-05
|
|
|
INSR
|
[NCBI]
|
8.28384e-05
|
|
|
FMD
|
[NCBI]
|
7.40438e-05
|
|
|
CNC1
|
[NCBI]
|
6.09211e-05
|
|
|
AR
|
[NCBI]
|
4.85609e-05
|
|
|
SRD5A1
|
[NCBI]
|
4.76758e-05
|
|
|
EIG
|
[NCBI]
|
3.92096e-05
|
|
|
3-@beta-hydroxysteroid dehydrogenase, type ii, deficiency of
|
[NCBI]
|
3.6797e-05
|
|
|
KLK3
|
[NCBI]
|
3.33918e-05
|
|
|
SRD5A2
|
[NCBI]
|
3.1778e-05
|
|
|
NR5A1
|
[NCBI]
|
3.05538e-05
|
|
|
GIP
|
[NCBI]
|
3.01413e-05
|
|
|
GCCR
|
[NCBI]
|
2.78948e-05
|
|
|
GDXY
|
[NCBI]
|
2.78948e-05
|
|
|
NR0B1
|
[NCBI]
|
2.78948e-05
|
|
|
GNRH1
|
[NCBI]
|
2.54622e-05
|
|
|
glycogen storage disease i
|
[NCBI]
|
2.25207e-05
|
|
|
porphyria cutanea tarda
|
[NCBI]
|
2.21999e-05
|
|
|
TNF
|
[NCBI]
|
2.18282e-05
|
|
|
cortisol 11-beta-ketoreductase deficiency
|
[NCBI]
|
2.10191e-05
|
|
|
STAR
|
[NCBI]
|
1.9379e-05
|
|
|
SERPINA6
|
[NCBI]
|
1.72411e-05
|
|
|
CRH
|
[NCBI]
|
1.33762e-05
|
|
|
CP
|
[NCBI]
|
1.02676e-05
|
|
|
SLE
|
[NCBI]
|
9.43832e-06
|
|