Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Androgen-Insensitivity Syndrome	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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