Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Hydroxyprogesterones [NCBI]

Gene


 Gene Link Information
Gain		 01
PRL [NCBI] 2.29566e-05
CYP2C8 [NCBI] 9.14788e-06
SHBG [NCBI] 7.47707e-06
CYP2C9 [NCBI] 7.28306e-06
TAT [NCBI] 3.05544e-06
UGT2B17 [NCBI] 1.91324e-06
HSD3B1 [NCBI] 1.86151e-06
BMP15 [NCBI] 1.60555e-06
FSHR [NCBI] 1.6033e-06
GDF9 [NCBI] 1.56972e-06
CYP21A2 [NCBI] 1.52951e-06
CCRK [NCBI] 1.35963e-06
CDK7 [NCBI] 1.32203e-06
PAEP [NCBI] 1.30251e-06
CP [NCBI] 1.24481e-06
PGR [NCBI] 1.1402e-06
TRH [NCBI] 7.73956e-07
AR [NCBI] 7.24265e-07
VEGFA [NCBI] 7.23866e-07
VIP [NCBI] 7.07742e-07
EGF [NCBI] 4.07519e-07



OMIM


 OMIM Link Information
gain		 01
PCOS1 [NCBI] 0.00181128
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency [NCBI] 0.000796048
17-@beta hydroxysteroid dehydrogenase iii deficiency [NCBI] 0.000419394
adrenal hyperplasia, congenital, due to steroid 11-beta-hydroxylase deficiency [NCBI] 0.000244225
PRL [NCBI] 0.000154971
AIS [NCBI] 0.000150503
monilethrix [NCBI] 0.000127632
adrenal hyperplasia, congenital, due to 17-alpha-hydroxylase deficiency [NCBI] 0.000105891
HAE [NCBI] 8.30238e-05
BWS [NCBI] 5.9401e-05
SHBG [NCBI] 5.78589e-05
SLOS [NCBI] 5.66894e-05
SERPINA6 [NCBI] 2.64304e-05
3-@beta-hydroxysteroid dehydrogenase, type ii, deficiency of [NCBI] 2.34094e-05
CYP11B1 [NCBI] 2.20981e-05
CYP19A1 [NCBI] 1.72579e-05
CP [NCBI] 8.00524e-06
PGR [NCBI] 7.33207e-06
GNRH1 [NCBI] 3.7294e-06
CRH [NCBI] 3.45534e-06
EGF [NCBI] 3.09547e-06
VEGF [NCBI] 2.54057e-06
AR [NCBI] 5.96093e-07
VIP [NCBI] 1.92179e-07



Database Center for Life Science