Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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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