Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Adrenocortical Hyperfunction	[NCBI]

Gene	Link	Information Gain
CRH	[NCBI]	3.00505e-05
PTH	[NCBI]	2.01011e-05
PDE11A	[NCBI]	1.28325e-05
CYP11A1	[NCBI]	1.03859e-05
LHCGR	[NCBI]	1.03859e-05
HSD11B2	[NCBI]	8.80164e-06
ABCD1	[NCBI]	8.1274e-06
NR3C1	[NCBI]	8.02603e-06
HP	[NCBI]	6.59124e-06
TOP2A	[NCBI]	5.95638e-06
VIP	[NCBI]	4.95583e-06
LPL	[NCBI]	4.4347e-06
AVP	[NCBI]	4.41807e-06
PRL	[NCBI]	3.26419e-06

OMIM	Link	Information gain
acanthosis nigricans	[NCBI]	0.00116675
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency	[NCBI]	0.000300208
AIMAH	[NCBI]	0.000162313
GCCR	[NCBI]	0.000154815
GRA	[NCBI]	0.000148143
hypersecretion of adrenal androgens, familial	[NCBI]	0.000145155
CRH	[NCBI]	0.000130323
cortisone reductase deficiency	[NCBI]	0.000104604
corticosterone methyloxidase type ii deficiency	[NCBI]	8.93796e-05
lipoid congenital adrenal hyperplasia	[NCBI]	8.45465e-05
adrenal hyperplasia, congenital, due to steroid 11-beta-hydroxylase deficiency	[NCBI]	8.0832e-05
adrenal hyperplasia, congenital, due to 17-alpha-hydroxylase deficiency	[NCBI]	8.0832e-05
ADRBK1	[NCBI]	6.24949e-05
PDE11A	[NCBI]	6.24949e-05
MEN2A	[NCBI]	5.64487e-05
CYP11A1	[NCBI]	5.63228e-05
PTH	[NCBI]	3.53361e-05
GNAS	[NCBI]	3.13189e-05
temporal arteritis	[NCBI]	3.03278e-05
HP	[NCBI]	1.83723e-05
GNRH1	[NCBI]	1.76303e-05
VIP	[NCBI]	8.58186e-06
LPL	[NCBI]	6.76066e-06
AVP	[NCBI]	4.05919e-06
PRL	[NCBI]	1.58055e-06