Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Gynecomastia	[NCBI]

Gene	Link	Information Gain
WTS	[NCBI]	0.000438875
PRL	[NCBI]	7.82171e-05
AR	[NCBI]	4.04964e-05
CYP19A1	[NCBI]	3.46779e-05
CGNL1	[NCBI]	1.7201e-05
PHF6	[NCBI]	1.16194e-05
HSD17B3	[NCBI]	1.07787e-05
TRPM7	[NCBI]	1.00645e-05
LHCGR	[NCBI]	9.17395e-06
PRLR	[NCBI]	8.53051e-06
CDR1	[NCBI]	8.50098e-06
NGFR	[NCBI]	6.96656e-06
PIP	[NCBI]	6.91965e-06
S100A4	[NCBI]	6.80777e-06
SRY	[NCBI]	6.4395e-06
APOD	[NCBI]	6.11567e-06
IGFBP3	[NCBI]	5.87509e-06
CYP3A4	[NCBI]	5.12145e-06
MECP2	[NCBI]	5.11355e-06
TRH	[NCBI]	3.65791e-06
CD68	[NCBI]	3.14267e-06
GFAP	[NCBI]	2.43993e-06
VWF	[NCBI]	2.43851e-06
PTGS2	[NCBI]	1.54945e-06

OMIM	Link	Information gain
WTS	[NCBI]	0.00425713
AEXS	[NCBI]	0.000952162
reifenstein syndrome	[NCBI]	0.00052356
17-@beta hydroxysteroid dehydrogenase iii deficiency	[NCBI]	0.000469052
pseudohermaphroditism, incomplete male, type i	[NCBI]	0.000436299
CYP19A1	[NCBI]	0.000332222
PJS	[NCBI]	0.000304934
SMAX1	[NCBI]	0.000271598
AIS	[NCBI]	0.000255502
PRL	[NCBI]	0.000244461
gynecomastia, familial	[NCBI]	0.000217359
AR	[NCBI]	0.000158788
PPSH	[NCBI]	0.000127254
infertile male syndrome	[NCBI]	9.30209e-05
ossified ear cartilages with mental deficiency, muscle wasting, and bony changes	[NCBI]	9.30209e-05
CGNL1	[NCBI]	8.21209e-05
TRS	[NCBI]	7.31286e-05
TMOD3	[NCBI]	6.83427e-05
TRPM7	[NCBI]	5.97685e-05
MRXHF1	[NCBI]	5.54412e-05
HSD17B3	[NCBI]	5.35982e-05
hepatocellular carcinoma	[NCBI]	5.25767e-05
3-@beta-hydroxysteroid dehydrogenase, type ii, deficiency of	[NCBI]	4.63428e-05
SLE	[NCBI]	4.4589e-05
KLK3	[NCBI]	3.96677e-05
alopecia, androgenetic	[NCBI]	3.5234e-05
SRY	[NCBI]	3.06244e-05
NGFR	[NCBI]	2.92572e-05
MECP2	[NCBI]	2.42334e-05
RTT	[NCBI]	2.01269e-05
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency	[NCBI]	1.99936e-05
GIST	[NCBI]	1.68861e-05
GNRH1	[NCBI]	1.51112e-05
GFAP	[NCBI]	1.34833e-06