Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Scrotum	[NCBI]

Gene	Link	Information Gain
AR	[NCBI]	1.97583e-05
FGD1	[NCBI]	1.46953e-05
INSL3	[NCBI]	1.13073e-05
MUC2	[NCBI]	9.70146e-06
SRD5A1	[NCBI]	6.64873e-06
PAX7	[NCBI]	6.01627e-06
EBAG9	[NCBI]	5.5958e-06
DSG1	[NCBI]	5.29205e-06
ATXN3	[NCBI]	5.13862e-06
PAX3	[NCBI]	4.68862e-06
CDKN2B	[NCBI]	4.33886e-06
PTPN11	[NCBI]	3.56266e-06
CREBBP	[NCBI]	3.5341e-06
AFP	[NCBI]	2.81158e-06
CD68	[NCBI]	2.77839e-06
TRH	[NCBI]	2.49238e-06
CFTR	[NCBI]	2.1355e-06
PTH	[NCBI]	1.82838e-06
NGF	[NCBI]	1.42795e-06

OMIM	Link	Information gain
genitopatellar syndrome	[NCBI]	0.00269526
faciogenital dysplasia	[NCBI]	0.00123526
acne inversa, familial	[NCBI]	0.0012021
robinow syndrome, autosomal dominant	[NCBI]	0.000779239
OD	[NCBI]	0.000720545
SMAX1	[NCBI]	0.000367511
emphysema, congenital, with deafness, penoscrotal web, and mental retardation	[NCBI]	0.000211181
paget disease, extramammary	[NCBI]	0.000211181
S PEAK SYNDROME	[NCBI]	0.00017192
aarskog syndrome	[NCBI]	0.000157111
cutis gyrata syndrome of beare and stevenson	[NCBI]	0.000157111
AR	[NCBI]	0.000140813
AIS	[NCBI]	0.000139821
frontonasal dysplasia	[NCBI]	0.000122361
DDD	[NCBI]	0.000113837
PMDS	[NCBI]	0.000109324
PPSH	[NCBI]	0.000107315
lipoid proteinosis of urbach and wiethe	[NCBI]	0.000107315
PPS	[NCBI]	9.75981e-05
FGD1	[NCBI]	9.66534e-05
EV	[NCBI]	6.75797e-05
CEACAM5	[NCBI]	4.23099e-05
FMF	[NCBI]	3.67911e-05
CREBBP	[NCBI]	3.30729e-05
SLE	[NCBI]	1.99617e-05
SHBG	[NCBI]	1.5928e-05
thrombocytopenic purpura, autoimmune	[NCBI]	1.38816e-05
CF	[NCBI]	1.03693e-05
AFP	[NCBI]	8.62094e-06
KLK3	[NCBI]	7.88786e-06
CFTR	[NCBI]	7.85148e-06
PTH	[NCBI]	2.83477e-06
NGFB	[NCBI]	1.0338e-06
VEGF	[NCBI]	2.78289e-07