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MeSH keywords -> Related genes, diseases (OMIM)


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01 Gonadotropins, Pituitary [NCBI]


Gene


Gene Link Information
Gain
01
PRL [NCBI] 0.000207411
MS [NCBI] 0.000111788
SHBG [NCBI] 1.53465e-05
EGF [NCBI] 8.34026e-06
TRH [NCBI] 8.2723e-06
NPY [NCBI] 7.81982e-06
POMC [NCBI] 5.18135e-06
KAL1 [NCBI] 4.43637e-06
TBX19 [NCBI] 3.3294e-06
KISS1R [NCBI] 2.76755e-06
AR [NCBI] 2.6143e-06
PTH [NCBI] 1.98118e-06
NELF [NCBI] 1.68736e-06
GNRH2 [NCBI] 1.5928e-06
TH [NCBI] 1.57008e-06
HSD3B2 [NCBI] 1.37299e-06
SALL1 [NCBI] 1.36805e-06
GNRH1 [NCBI] 1.33579e-06
HESX1 [NCBI] 1.33579e-06
POU3F2 [NCBI] 1.27068e-06
ADRBK2 [NCBI] 1.21841e-06
CLEC3B [NCBI] 1.21289e-06
LHCGR [NCBI] 1.18936e-06
FSHR [NCBI] 1.15869e-06
GNRHR [NCBI] 1.14778e-06
KISS1 [NCBI] 1.08692e-06
HES1 [NCBI] 1.06259e-06
PITX1 [NCBI] 1.03469e-06
GHRH [NCBI] 1.03054e-06
PRKAR1A [NCBI] 9.95885e-07
ATXN3 [NCBI] 9.68502e-07
POU1F1 [NCBI] 9.29328e-07
GFAP [NCBI] 9.06228e-07
CYP19A1 [NCBI] 9.05282e-07
IGFBP3 [NCBI] 8.53036e-07
PAM [NCBI] 8.25963e-07
CHGA [NCBI] 7.81711e-07
GRP [NCBI] 7.2383e-07
INS [NCBI] 7.18003e-07
PGR [NCBI] 7.00515e-07
TGFBR1 [NCBI] 6.67783e-07
CTGF [NCBI] 6.10737e-07
AHR [NCBI] 5.84306e-07
CTSL1 [NCBI] 5.29908e-07
HGF [NCBI] 3.45846e-07
TNF [NCBI] 3.15691e-07
VIP [NCBI] 2.92859e-07
CCK [NCBI] 2.73606e-07




OMIM


OMIM Link Information
gain
01
PRL [NCBI] 0.00194522
anosmia, congenital [NCBI] 0.00192174
chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism [NCBI] 0.00179377
PHP [NCBI] 0.00179377
cerebellar ataxia and hypogonadotropic hypogonadism [NCBI] 0.00169869
hypogonadotropic hypogonadism [NCBI] 0.00043579
KAL2 [NCBI] 0.000321314
GNRH1 [NCBI] 0.000254173
eunuchoidism, familial hypogonadotropic [NCBI] 0.000246475
precocious puberty, male-limited [NCBI] 0.000233294
POF1 [NCBI] 0.000196361
kallmann syndrome with spastic paraplegia [NCBI] 0.000170598
fertile eunuch syndrome [NCBI] 0.000127109
cardiomyopathy, congestive, with hypergonadotropic hypogonadism [NCBI] 0.000127109
SHBG [NCBI] 0.000124513
fragile x mental retardation syndrome [NCBI] 0.000123869
RA [NCBI] 9.11767e-05
pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities [NCBI] 9.04109e-05
pituitary dwarfism due to isolated growth hormone deficiency, autosomal dominant [NCBI] 8.86688e-05
17-@beta hydroxysteroid dehydrogenase iii deficiency [NCBI] 8.55445e-05
PHS [NCBI] 8.55445e-05
pituitary dwarfism i [NCBI] 8.28033e-05
BPES [NCBI] 7.61596e-05
TBS [NCBI] 7.43233e-05
SLE [NCBI] 5.56567e-05
BBS [NCBI] 5.17155e-05
FFI [NCBI] 4.62767e-05
MAS [NCBI] 4.51144e-05
AIS [NCBI] 3.43647e-05
dystrophia myotonica 1 [NCBI] 3.41042e-05
KAL1 [NCBI] 3.36053e-05
ADCYAP1 [NCBI] 3.25275e-05
POMC [NCBI] 2.89307e-05
TNF [NCBI] 2.32228e-05
VEGF [NCBI] 2.07903e-05
CF [NCBI] 1.81336e-05
3-@beta-hydroxysteroid dehydrogenase, type ii, deficiency of [NCBI] 1.6277e-05
NPY [NCBI] 1.59331e-05
LHCGR [NCBI] 1.12587e-05
PRLH [NCBI] 9.9258e-06
GHRH [NCBI] 8.04644e-06
CEACAM5 [NCBI] 7.32495e-06
CJD [NCBI] 7.14333e-06
PAM [NCBI] 7.10555e-06
PLAUR [NCBI] 6.85694e-06
AVP [NCBI] 6.76507e-06
CCK [NCBI] 5.39128e-06
PRNP [NCBI] 4.71776e-06
VIP [NCBI] 4.47332e-06
EGF [NCBI] 3.50662e-06
INS [NCBI] 2.53827e-06
HGF [NCBI] 2.17274e-06
KLK3 [NCBI] 1.95588e-06
PGR [NCBI] 1.70649e-06
GAL [NCBI] 1.67302e-06
CTGF [NCBI] 1.16371e-06
GFAP [NCBI] 9.47518e-07
AR [NCBI] 5.37488e-07
PTH [NCBI] 5.05437e-07
TH [NCBI] 1.14616e-07
AHR [NCBI] 1.13494e-07
AD [NCBI] 1.23991e-08
CRH [NCBI] 2.30948e-09




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