Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Scrotum [NCBI]

Gene


 Gene Link Information
Gain		 01
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


 OMIM Link Information
gain		 01
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



Database Center for Life Science