Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Adrenocortical Hyperfunction [NCBI]

Gene


 Gene Link Information
Gain		 01
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


 OMIM Link Information
gain		 01
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



Database Center for Life Science