MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Androgen-Insensitivity Syndrome
[NCBI]
Gene
Gene
Link
Information
Gain
01
AR
[NCBI]
0.00161827
NCOA2
[NCBI]
4.24533e-05
SHBG
[NCBI]
2.24637e-05
AMH
[NCBI]
1.84978e-05
SRY
[NCBI]
9.7943e-06
UXT
[NCBI]
8.85844e-06
NAP1L1
[NCBI]
8.85844e-06
RNF4
[NCBI]
8.53088e-06
A1BG
[NCBI]
8.388e-06
HEPH
[NCBI]
7.71684e-06
ALDH1A1
[NCBI]
7.38217e-06
NR5A1
[NCBI]
6.91965e-06
ZFY
[NCBI]
6.65268e-06
SET
[NCBI]
6.33812e-06
TSPY1
[NCBI]
6.14468e-06
NKX3-1
[NCBI]
5.87513e-06
NCOA4
[NCBI]
5.2577e-06
MSN
[NCBI]
5.15358e-06
SRD5A2
[NCBI]
4.74458e-06
SP1
[NCBI]
4.40478e-06
CREBBP
[NCBI]
3.35702e-06
OSM
[NCBI]
3.04823e-06
CD99
[NCBI]
3.03753e-06
MUC1
[NCBI]
2.17835e-06
EGF
[NCBI]
7.21458e-07
GFAP
[NCBI]
3.49189e-07
NGF
[NCBI]
3.0584e-07
OMIM
OMIM
Link
Information
gain
01
AIS
[NCBI]
0.0118645
AR
[NCBI]
0.00554982
PPSH
[NCBI]
0.000232632
reifenstein syndrome
[NCBI]
0.000136341
androgen insensitivity syndrome due to coactivator deficiency
[NCBI]
0.000106668
AMH
[NCBI]
9.25487e-05
SHBG
[NCBI]
8.04423e-05
gynecomastia, familial
[NCBI]
7.57576e-05
infertile male syndrome
[NCBI]
7.57576e-05
pseudohermaphroditism, incomplete male, type i
[NCBI]
6.29565e-05
TRS
[NCBI]
5.5954e-05
TSPY
[NCBI]
4.92794e-05
17-@beta hydroxysteroid dehydrogenase iii deficiency
[NCBI]
4.74246e-05
SMAX1
[NCBI]
4.53717e-05
MSN
[NCBI]
4.34106e-05
adrenal hyperplasia, congenital, due to 17-alpha-hydroxylase deficiency
[NCBI]
4.27326e-05
DHH
[NCBI]
3.41386e-05
HEPH
[NCBI]
3.41386e-05
PJS
[NCBI]
3.3652e-05
GATA4
[NCBI]
3.25645e-05
GDXY
[NCBI]
2.37349e-05
LHCGR
[NCBI]
2.24037e-05
OSM
[NCBI]
9.27179e-06
EGF
[NCBI]
8.79975e-06
NGFB
[NCBI]
5.32347e-06
GFAP
[NCBI]
4.55989e-06
Database Center for Life Science