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01 Hypogonadism [NCBI]

Gene


 Gene Link Information
Gain		 01
GNRHR [NCBI] 0.000449073
MEHMO [NCBI] 0.000438875
MCS [NCBI] 0.000378131
KISS1R [NCBI] 0.000319928
KAL1 [NCBI] 0.000290861
NR0B1 [NCBI] 0.000218386
PRL [NCBI] 0.000140765
KISS1 [NCBI] 0.000128275
SHBG [NCBI] 0.000104185
LHB [NCBI] 6.41159e-05
FGFR1 [NCBI] 6.14715e-05
NELF [NCBI] 6.07159e-05
TRH [NCBI] 3.19202e-05
PHF6 [NCBI] 3.13747e-05
SRY [NCBI] 2.99241e-05
PROK2 [NCBI] 2.82644e-05
GNRH1 [NCBI] 2.70808e-05
PROKR2 [NCBI] 1.93115e-05
PDE5A [NCBI] 1.89581e-05
AR [NCBI] 1.77873e-05
BBS4 [NCBI] 1.62425e-05
EBF2 [NCBI] 1.39467e-05
LBX2 [NCBI] 1.39467e-05
PIK3AP1 [NCBI] 1.39467e-05
FGF8 [NCBI] 1.22425e-05
GTF2A1L [NCBI] 1.06687e-05
RAB3GAP1 [NCBI] 1.00857e-05
HFE [NCBI] 1.00553e-05
AMH [NCBI] 9.96972e-06
GABRG3 [NCBI] 9.30707e-06
CUL4B [NCBI] 9.02004e-06
XG [NCBI] 9.02004e-06
USP26 [NCBI] 8.7744e-06
MAGEB1 [NCBI] 8.5597e-06
CYP19A1 [NCBI] 8.40381e-06
NPY1R [NCBI] 8.36902e-06
FSHB [NCBI] 8.36902e-06
RPL7A [NCBI] 8.04171e-06
SF1 [NCBI] 7.89896e-06
GABRR2 [NCBI] 7.76724e-06
FGF23 [NCBI] 7.70742e-06
HSD17B3 [NCBI] 7.53094e-06
OXTR [NCBI] 7.42406e-06
VDR [NCBI] 7.32746e-06
CANX [NCBI] 7.3235e-06
PROP1 [NCBI] 7.05326e-06
BBS2 [NCBI] 6.8944e-06
CHD7 [NCBI] 6.74916e-06
ALMS1 [NCBI] 6.55231e-06
NR5A1 [NCBI] 6.43276e-06
LEP [NCBI] 6.33766e-06
ZFY [NCBI] 6.16643e-06
CPE [NCBI] 6.07067e-06
POU3F2 [NCBI] 6.07067e-06
HESX1 [NCBI] 5.98008e-06
LHCGR [NCBI] 5.93656e-06
INHBB [NCBI] 5.93656e-06
TSPY1 [NCBI] 5.65995e-06
GDF5 [NCBI] 5.42271e-06
INHA [NCBI] 5.39141e-06
PTH1R [NCBI] 5.33054e-06
FSHR [NCBI] 5.30093e-06
NPY [NCBI] 5.26202e-06
HFE2 [NCBI] 5.21512e-06
NTN1 [NCBI] 5.21512e-06
TYMP [NCBI] 5.10721e-06
WFDC5 [NCBI] 5.0558e-06
SOX2 [NCBI] 5.03067e-06
STAR [NCBI] 4.57622e-06
VKORC1 [NCBI] 4.48439e-06
INSL3 [NCBI] 4.43168e-06
OPA1 [NCBI] 4.43168e-06
POLG [NCBI] 4.29899e-06
MSTN [NCBI] 4.14715e-06
EIF4EBP1 [NCBI] 4.0218e-06
NOG [NCBI] 3.77425e-06
CRH [NCBI] 3.63195e-06
LEPR [NCBI] 3.50154e-06
CYP17A1 [NCBI] 3.15809e-06
LPL [NCBI] 2.88507e-06
FOLH1 [NCBI] 2.72142e-06
DMPK [NCBI] 2.43219e-06
INS [NCBI] 2.24058e-06
PTH [NCBI] 1.68395e-06
GJB2 [NCBI] 1.44349e-06
LIF [NCBI] 1.39938e-06
PTGS1 [NCBI] 1.23538e-06
IL1B [NCBI] 1.20922e-06
TNFRSF11B [NCBI] 1.19724e-06
CXCL12 [NCBI] 1.12977e-06
CETP [NCBI] 1.12977e-06
NOS3 [NCBI] 5.02499e-07
GFAP [NCBI] 1.36831e-07
EGF [NCBI] 6.09975e-08
PCNA [NCBI] 3.85599e-08
PTGS2 [NCBI] 2.66988e-08
CFTR [NCBI] 5.55672e-09



OMIM


 OMIM Link Information
gain		 01
hypogonadotropic hypogonadism [NCBI] 0.00713431
cerebellar ataxia and hypogonadotropic hypogonadism [NCBI] 0.00608418
chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism [NCBI] 0.00608418
MEHMO [NCBI] 0.00345077
MBS [NCBI] 0.00275757
hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndrome [NCBI] 0.00258184
johnson neuroectodermal syndrome [NCBI] 0.00222882
GNRHR [NCBI] 0.00151874
KAL2 [NCBI] 0.00123262
KAL1 [NCBI] 0.00112912
anosmia, congenital [NCBI] 0.0011193
NR0B1 [NCBI] 0.000921003
MCS [NCBI] 0.000856564
coloboma-obesity-hypogenitalism-mental retardation syndrome [NCBI] 0.000856564
HHG [NCBI] 0.000639274
ketoaciduria with mental deficiency and other features [NCBI] 0.000639274
scholte syndrome [NCBI] 0.000639274
RA [NCBI] 0.000571937
WTS [NCBI] 0.000557676
AHC [NCBI] 0.000550243
ichthyosis, x-linked [NCBI] 0.00038081
cardiomyopathy, congestive, with hypergonadotropic hypogonadism [NCBI] 0.000380425
BFLS [NCBI] 0.000373608
gonadal dysgenesis, xx type, with deafness [NCBI] 0.000368318
ear, patella, short stature syndrome [NCBI] 0.000351483
PRL [NCBI] 0.000331297
PWS [NCBI] 0.000327428
SHBG [NCBI] 0.000324139
APS2 [NCBI] 0.000322762
GNRH1 [NCBI] 0.000321493
SLE [NCBI] 0.000290774
eunuchoidism, familial hypogonadotropic [NCBI] 0.000290717
ichthyosis and male hypogonadism [NCBI] 0.000285222
BBS [NCBI] 0.000282166
robinow syndrome, autosomal dominant [NCBI] 0.000252679
GPR54 [NCBI] 0.000233305
LHB [NCBI] 0.000233305
MRXHF1 [NCBI] 0.000200479
martsolf syndrome [NCBI] 0.000192633
NELF [NCBI] 0.000191441
cerebellar ataxia and hypergonadotropic hypogonadism [NCBI] 0.000190084
craniosynostosis-mental retardation syndrome of lin and gettig [NCBI] 0.000190084
retinitis pigmentosa, deafness, mental retardation, and hypogonadism [NCBI] 0.000190084
FGFR1 [NCBI] 0.000168214
cardiogenital syndrome [NCBI] 0.000159175
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 1 [NCBI] 0.000151616
JH [NCBI] 0.000151616
intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies [NCBI] 0.000145231
FSHB [NCBI] 0.000134591
WARBM [NCBI] 0.000117434
charge syndrome [NCBI] 0.000116691
KLK3 [NCBI] 0.000100775
17-@beta hydroxysteroid dehydrogenase iii deficiency [NCBI] 9.51995e-05
hyperzincemia with functional zinc depletion [NCBI] 9.50102e-05
kallmann syndrome with spastic paraplegia [NCBI] 9.50102e-05
mental retardation syndrome, belgian type [NCBI] 9.50102e-05
hypogonadism, primary, and partial alopecia [NCBI] 9.50102e-05
multicore myopathy with mental retardation, short stature, and hypogonadotropic hypogonadism [NCBI] 9.50102e-05
hypogonadism-cataract syndrome [NCBI] 9.50102e-05
retinitis pigmentosa inversa with deafness [NCBI] 9.50102e-05
brachytelephalangy with characteristic facies and kallmann syndrome [NCBI] 9.50102e-05
HFE [NCBI] 8.83496e-05
CYP19A1 [NCBI] 8.76748e-05
UMS [NCBI] 8.55159e-05
adrenal hyperplasia, congenital, due to 17-alpha-hydroxylase deficiency [NCBI] 8.55159e-05
BBS4 [NCBI] 8.03078e-05
ALMS [NCBI] 7.56616e-05
MELAS [NCBI] 7.56616e-05
mental retardation, x-linked, with short stature, small testes, muscle wasting, and tremor [NCBI] 7.25837e-05
hypogonadism, male [NCBI] 7.25837e-05
DHS [NCBI] 7.25837e-05
biemond syndrome ii [NCBI] 7.25837e-05
proprotein convertase 1 deficiency [NCBI] 7.25837e-05
AD [NCBI] 6.42569e-05
cerebellar ataxia and ectodermal dysplasia [NCBI] 6.41476e-05
alopecia-mental retardation syndrome with convulsions and hypergonadotropic hypogonadism [NCBI] 6.41476e-05
arhinia, choanal atresia, and microphthalmia [NCBI] 6.41476e-05
retinopathy, pigmentary, and mental retardation [NCBI] 6.41476e-05
fertile eunuch syndrome [NCBI] 6.41476e-05
LBX2 [NCBI] 6.37718e-05
suppressor of variegation 3-9, drosophila, homolog of, 2 [NCBI] 6.37718e-05
PROP1 [NCBI] 6.32456e-05
XPA [NCBI] 5.94276e-05
cardiomyopathy-hypogonadism-collagenoma syndrome [NCBI] 5.86855e-05
hypogonadism, male [NCBI] 5.86855e-05
roifman syndrome [NCBI] 5.86855e-05
DM2 [NCBI] 5.43786e-05
ALD [NCBI] 5.40037e-05
BJS [NCBI] 5.14177e-05
pseudohermaphroditism, incomplete male, type i [NCBI] 5.14177e-05
EBF2 [NCBI] 5.00073e-05
LHCGR [NCBI] 4.97654e-05
follicle-stimulating hormone deficiency, isolated [NCBI] 4.87494e-05
palmoplantar hyperkeratosis with squamous cell carcinoma of skin and sex reversal [NCBI] 4.87494e-05
RAB3GAP1 [NCBI] 4.48221e-05
MAGEB1 [NCBI] 4.48221e-05
SUV39H1 [NCBI] 4.48221e-05
reifenstein syndrome [NCBI] 4.44864e-05
NHLH2 [NCBI] 4.14605e-05
BBS2 [NCBI] 4.14605e-05
CUL4B [NCBI] 4.14605e-05
EGF [NCBI] 4.11618e-05
de sanctis-cacchione syndrome [NCBI] 4.115e-05
pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities [NCBI] 3.97204e-05
PHF6 [NCBI] 3.8965e-05
MERRF [NCBI] 3.84141e-05
pituitary dwarfism due to isolated growth hormone deficiency, autosomal dominant [NCBI] 3.72121e-05
MTTH [NCBI] 3.69796e-05
HSD17B3 [NCBI] 3.53313e-05
KISS1 [NCBI] 3.53313e-05
pituitary dwarfism iii [NCBI] 3.5064e-05
xanthinuria, type i [NCBI] 3.5064e-05
coenzyme q10 deficiency [NCBI] 3.5064e-05
EEC3 [NCBI] 3.40963e-05
PCSK1 [NCBI] 3.39226e-05
MCPH1 [NCBI] 3.23335e-05
CDPX1 [NCBI] 3.23335e-05
MG [NCBI] 3.19105e-05
ACLS [NCBI] 2.74536e-05
LEP [NCBI] 2.69367e-05
POF1 [NCBI] 2.68761e-05
RIEG1 [NCBI] 2.63217e-05
AMH [NCBI] 2.48712e-05
leopard syndrome 1 [NCBI] 2.47816e-05
MSS [NCBI] 2.43048e-05
GHRL [NCBI] 2.24246e-05
TP73L [NCBI] 2.24246e-05
PITX2 [NCBI] 2.20432e-05
NR5A1 [NCBI] 2.20432e-05
growth hormone insensitivity syndrome [NCBI] 2.17552e-05
INSL3 [NCBI] 2.1677e-05
MDD [NCBI] 2.11759e-05
PTH [NCBI] 2.04815e-05
AIS [NCBI] 2.04171e-05
GDXY [NCBI] 1.94604e-05
CYP17A1 [NCBI] 1.91842e-05
WFS1 [NCBI] 1.89897e-05
PCNA [NCBI] 1.87465e-05
POLG [NCBI] 1.81587e-05
ATRX [NCBI] 1.792e-05
CES [NCBI] 1.72587e-05
galactosemia [NCBI] 1.69931e-05
RTS [NCBI] 1.62308e-05
HS [NCBI] 1.34516e-05
ABCD1 [NCBI] 1.34516e-05
ALGS1 [NCBI] 1.32308e-05
SRY [NCBI] 1.31805e-05
GFAP [NCBI] 1.29933e-05
AR [NCBI] 1.23157e-05
LEPR [NCBI] 1.22994e-05
MTTL1 [NCBI] 1.15088e-05
STAR [NCBI] 1.14024e-05
SLS [NCBI] 1.1357e-05
NS1 [NCBI] 9.03642e-06
APS1 [NCBI] 8.34553e-06
VDR [NCBI] 8.24246e-06
von willebrand disease [NCBI] 7.95345e-06
MAS [NCBI] 6.66577e-06
RP [NCBI] 4.56295e-06
CD [NCBI] 4.36025e-06
KSS [NCBI] 4.32696e-06
EIG [NCBI] 4.2082e-06
FA [NCBI] 5.80149e-07
NPY [NCBI] 3.63762e-07
CVID [NCBI] 3.67379e-09
LPL [NCBI] 3.4848e-09
TNFRSF11B [NCBI] 6.93512e-10



Database Center for Life Science