Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Mineralocorticoids	[NCBI]

Gene	Link	Information Gain
HSD11B2	[NCBI]	5.73002e-05
SGK1	[NCBI]	1.55451e-05
NR3C2	[NCBI]	1.00007e-05
HSD11B1	[NCBI]	7.14059e-06
AVP	[NCBI]	6.16609e-06
PIH	[NCBI]	4.52683e-06
CYP11B1	[NCBI]	3.71973e-06
CYP11B2	[NCBI]	3.07161e-06
AQP2	[NCBI]	2.73748e-06
ADM	[NCBI]	2.53138e-06
POMC	[NCBI]	2.14353e-06
CASP8AP2	[NCBI]	1.86351e-06
FAF1	[NCBI]	1.71619e-06
NDRG2	[NCBI]	1.70389e-06
KLK1	[NCBI]	1.5925e-06
AKR1C3	[NCBI]	1.55557e-06
ACTG1	[NCBI]	1.49976e-06
UGT2B7	[NCBI]	1.49976e-06
SCNN1B	[NCBI]	1.49422e-06
NR1I2	[NCBI]	1.49422e-06
KCNJ1	[NCBI]	1.4888e-06
CYP21A2	[NCBI]	1.36614e-06
ACTA1	[NCBI]	1.34497e-06
DAXX	[NCBI]	1.32828e-06
NCOA2	[NCBI]	1.27635e-06
SCARB1	[NCBI]	1.17336e-06
STAR	[NCBI]	1.13168e-06
SRY	[NCBI]	1.12888e-06
MDM2	[NCBI]	1.08312e-06
SLC9A3	[NCBI]	1.04921e-06
EGF	[NCBI]	8.58256e-07
CETP	[NCBI]	7.98245e-07
BDNF	[NCBI]	5.6568e-07
APOE	[NCBI]	5.41758e-07
EGFR	[NCBI]	4.31175e-07
PTH	[NCBI]	4.11146e-07

OMIM	Link	Information gain
cortisol 11-beta-ketoreductase deficiency	[NCBI]	0.00168653
AME2	[NCBI]	0.000526777
adrenal hyperplasia, congenital, due to 17-alpha-hydroxylase deficiency	[NCBI]	0.000235565
GRA	[NCBI]	0.000184091
cortisone reductase deficiency	[NCBI]	0.000129427
liddle syndrome	[NCBI]	0.000112624
GCCD1	[NCBI]	0.000105839
PHA2	[NCBI]	0.000101821
adrenal hyperplasia, congenital, due to steroid 11-beta-hydroxylase deficiency	[NCBI]	9.94913e-05
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency	[NCBI]	9.48068e-05
APC	[NCBI]	8.42651e-05
hypertension, essential	[NCBI]	7.77961e-05
HSD11B1	[NCBI]	5.18175e-05
CYP11B1	[NCBI]	4.91332e-05
AVP	[NCBI]	4.71302e-05
AQP2	[NCBI]	3.81195e-05
ADM	[NCBI]	2.29234e-05
NR3C2	[NCBI]	2.18084e-05
CYP11B2	[NCBI]	1.95371e-05
GCCR	[NCBI]	1.57637e-05
NPPA	[NCBI]	1.36719e-05
POMC	[NCBI]	1.31487e-05
NR1I2	[NCBI]	8.16691e-06
STAR	[NCBI]	7.52506e-06
CRH	[NCBI]	1.94461e-06
EGF	[NCBI]	1.37799e-06
PTH	[NCBI]	8.41927e-07
APOE	[NCBI]	2.65793e-07
BDNF	[NCBI]	4.30026e-08