Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


Query MeSH keywords list

01 Puberty, Precocious [NCBI]

Gene


 Gene Link Information
Gain		 01
LHCGR [NCBI] 0.000175593
GNAS [NCBI] 7.7417e-05
HSD3B2 [NCBI] 6.66477e-05
KISS1 [NCBI] 4.47291e-05
CYP21A2 [NCBI] 4.09005e-05
KISS1R [NCBI] 3.70349e-05
SHBG [NCBI] 3.57931e-05
NPY1R [NCBI] 2.26183e-05
AMH [NCBI] 2.19743e-05
PRL [NCBI] 2.132e-05
INHBB [NCBI] 1.75815e-05
FSHR [NCBI] 1.62814e-05
IRS1 [NCBI] 1.4539e-05
NR3C1 [NCBI] 1.28426e-05
ADRB3 [NCBI] 1.26724e-05
GTF2A1L [NCBI] 1.23171e-05
AFP [NCBI] 1.21714e-05
CYP19A1 [NCBI] 1.16435e-05
NPY5R [NCBI] 1.13001e-05
SORBS1 [NCBI] 1.06672e-05
INSM1 [NCBI] 1.00152e-05
GRM1 [NCBI] 9.84344e-06
NPY [NCBI] 9.74976e-06
IGFALS [NCBI] 9.54424e-06
MC2R [NCBI] 9.17528e-06
UGT2B15 [NCBI] 8.78173e-06
SERPINE1 [NCBI] 8.5249e-06
TNFAIP6 [NCBI] 8.0727e-06
AKR1C3 [NCBI] 7.96043e-06
GABRA1 [NCBI] 7.90696e-06
NR0B1 [NCBI] 7.02348e-06
AGTR2 [NCBI] 6.81733e-06
TRH [NCBI] 6.54733e-06
HSD11B1 [NCBI] 6.46786e-06
INHBA [NCBI] 6.33771e-06
STAR [NCBI] 6.19758e-06
GHRH [NCBI] 5.98156e-06
KAL1 [NCBI] 5.98156e-06
MC4R [NCBI] 5.77519e-06
IGF1R [NCBI] 5.04844e-06
STK11 [NCBI] 4.70181e-06
COL1A1 [NCBI] 4.62551e-06
IGF2 [NCBI] 4.41596e-06
IGFBP3 [NCBI] 4.30211e-06
AGTR1 [NCBI] 4.00722e-06
AHR [NCBI] 3.9135e-06
INS [NCBI] 3.77156e-06
CYP3A4 [NCBI] 3.56662e-06
IGF1 [NCBI] 3.44832e-06
TNFRSF11A [NCBI] 2.862e-06
ESR1 [NCBI] 2.74159e-06
TNFSF11 [NCBI] 2.64073e-06
TNFRSF11B [NCBI] 2.60189e-06
PTEN [NCBI] 1.63934e-06
AR [NCBI] 1.09608e-06
EPO [NCBI] 1.03281e-06
EGF [NCBI] 3.42096e-07



OMIM


 OMIM Link Information
gain		 01
precocious puberty [NCBI] 0.00758987
MAS [NCBI] 0.00314038
SRS [NCBI] 0.00146901
precocious puberty, male-limited [NCBI] 0.00104825
LHCGR [NCBI] 0.000900189
GNRH1 [NCBI] 0.000548482
varadi-papp syndrome [NCBI] 0.000462747
kabuki syndrome [NCBI] 0.00026551
AEXS [NCBI] 0.000154091
RA [NCBI] 0.000141934
SHBG [NCBI] 0.000125515
spastic paraplegia with precocious puberty [NCBI] 0.000115528
hypersecretion of adrenal androgens, familial [NCBI] 0.000115528
PJS [NCBI] 9.28289e-05
RSTS [NCBI] 8.88222e-05
CYP11B1 [NCBI] 8.78606e-05
AMH [NCBI] 8.41095e-05
boomerang dysplasia [NCBI] 6.67567e-05
AOI [NCBI] 5.98724e-05
enchondromatosis, multiple [NCBI] 5.40822e-05
septooptic dysplasia [NCBI] 5.31411e-05
WBS [NCBI] 5.23984e-05
SMMCI [NCBI] 5.2253e-05
adrenal hyperplasia, congenital, due to steroid 11-beta-hydroxylase deficiency [NCBI] 5.14123e-05
GAN1 [NCBI] 4.77762e-05
PRL [NCBI] 4.6662e-05
donohue syndrome [NCBI] 4.65298e-05
AHC [NCBI] 4.37923e-05
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency [NCBI] 4.18845e-05
MC2R [NCBI] 4.11418e-05
3-@beta-hydroxysteroid dehydrogenase, type ii, deficiency of [NCBI] 4.0381e-05
PHS [NCBI] 3.8715e-05
BRRS [NCBI] 3.38445e-05
NF1 [NCBI] 3.28067e-05
NR0B1 [NCBI] 3.14377e-05
AHO [NCBI] 2.60272e-05
IGFALS [NCBI] 2.30609e-05
AFP [NCBI] 2.29044e-05
STAR [NCBI] 2.28232e-05
NPY [NCBI] 1.96176e-05
GHR [NCBI] 1.90402e-05
PWS [NCBI] 1.854e-05
INS [NCBI] 1.41209e-05
GHRH [NCBI] 1.3497e-05
AS [NCBI] 9.59913e-06
TNFRSF11B [NCBI] 5.20701e-06
EGF [NCBI] 3.28568e-06
AR [NCBI] 1.20178e-07
APC [NCBI] 2.90861e-08
EPO [NCBI] 2.66967e-08



Database Center for Life Science