Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Cortodoxone [NCBI]

Gene


 Gene Link Information
Gain		 01
CYP11B1 [NCBI] 9.53102e-06
CYP11B2 [NCBI] 8.21858e-06
PRL [NCBI] 2.97469e-06
SCFV [NCBI] 2.1388e-06
TH [NCBI] 2.00979e-06
NR0B1 [NCBI] 1.87466e-06
CAPN10 [NCBI] 1.82099e-06
FSHR [NCBI] 1.75537e-06
HSD11B1 [NCBI] 1.72177e-06
HSD11B2 [NCBI] 1.67816e-06
PRKD1 [NCBI] 1.50357e-06
TAT [NCBI] 1.4908e-06
GHRL [NCBI] 1.47312e-06
STAR [NCBI] 1.44649e-06
NR3C1 [NCBI] 1.42422e-06
SHBG [NCBI] 1.20374e-06
AVP [NCBI] 8.56877e-07



OMIM


 OMIM Link Information
gain		 01
SRS [NCBI] 0.00149661
GRA [NCBI] 0.00047349
adrenal hyperplasia, congenital, due to steroid 11-beta-hydroxylase deficiency [NCBI] 0.000405989
por deficiency [NCBI] 0.000124318
CYP11B1 [NCBI] 0.000102973
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency [NCBI] 7.0674e-05
BWS [NCBI] 6.14204e-05
temporal arteritis [NCBI] 4.62856e-05
POR [NCBI] 3.31118e-05
CYP19A1 [NCBI] 2.30887e-05
cortisol 11-beta-ketoreductase deficiency [NCBI] 2.1785e-05
PRL [NCBI] 1.67932e-05
SERPINA6 [NCBI] 1.52759e-05
STAR [NCBI] 1.43792e-05
CRH [NCBI] 1.25621e-05
TH [NCBI] 1.16353e-05
SHBG [NCBI] 8.8121e-06
GNRH1 [NCBI] 8.78871e-06
RA [NCBI] 7.56737e-06
AVP [NCBI] 2.62721e-06



Database Center for Life Science