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01 Turner Syndrome [NCBI]

Gene


 Gene Link Information
Gain		 01
CGF1 [NCBI] 0.000438875
TNR1 [NCBI] 0.000438875
SHOX [NCBI] 0.00037931
SRY [NCBI] 0.000153169
TSPY1 [NCBI] 4.97828e-05
AR [NCBI] 3.3229e-05
EFHC2 [NCBI] 2.60404e-05
RPS4Y1 [NCBI] 2.30773e-05
RPS4X [NCBI] 2.30773e-05
TPO [NCBI] 1.59478e-05
SHBG [NCBI] 1.36914e-05
MAOA [NCBI] 1.31648e-05
PAEP [NCBI] 1.29552e-05
FMR1 [NCBI] 1.23921e-05
RAB5C [NCBI] 1.21139e-05
TRH [NCBI] 1.12481e-05
TG [NCBI] 1.1027e-05
IGFBP3 [NCBI] 1.05537e-05
SOX1 [NCBI] 9.64043e-06
CSF2RA [NCBI] 9.34128e-06
FRMD7 [NCBI] 9.08674e-06
FMO3 [NCBI] 8.41168e-06
BMP15 [NCBI] 8.05368e-06
BGN [NCBI] 7.92916e-06
CENPE [NCBI] 7.81312e-06
GDF9 [NCBI] 7.70449e-06
CENPC1 [NCBI] 7.65266e-06
ZFY [NCBI] 7.60237e-06
RBMY1A1 [NCBI] 7.32833e-06
DCN [NCBI] 7.24599e-06
AFP [NCBI] 7.17806e-06
AGTR2 [NCBI] 6.61557e-06
ADAM12 [NCBI] 6.5881e-06
FOXC2 [NCBI] 6.432e-06
KISS1 [NCBI] 5.92144e-06
RS1 [NCBI] 5.88515e-06
NKX2-5 [NCBI] 5.83214e-06
GHRH [NCBI] 5.78076e-06
KAL1 [NCBI] 5.78076e-06
DAZ1 [NCBI] 5.48757e-06
GHR [NCBI] 5.08713e-06
IGFBP1 [NCBI] 5.07605e-06
GIP [NCBI] 4.14869e-06
NOTCH1 [NCBI] 4.06351e-06
HNF1B [NCBI] 3.66712e-06
CFLAR [NCBI] 3.6172e-06
MECP2 [NCBI] 3.36617e-06
PRL [NCBI] 3.26009e-06
F2 [NCBI] 3.0332e-06
F5 [NCBI] 2.69898e-06
TNFRSF11A [NCBI] 2.67489e-06
TNFSF11 [NCBI] 2.45606e-06
TNFRSF11B [NCBI] 2.41768e-06
PTHLH [NCBI] 2.22461e-06
HLA-DRB1 [NCBI] 1.89114e-06
MTHFR [NCBI] 1.63046e-06
PCNA [NCBI] 6.99903e-07



OMIM


 OMIM Link Information
gain		 01
spatial visualization, aptitude for [NCBI] 0.0025497
CGF1 [NCBI] 0.00237459
gonadal dysgenesis, xx type, with deafness [NCBI] 0.00200421
NS1 [NCBI] 0.00159415
GBY [NCBI] 0.00132809
gordon syndrome [NCBI] 0.00114309
GDXY [NCBI] 0.0008283
brachydactyly-mental retardation syndrome [NCBI] 0.000607072
noonan syndrome 2 [NCBI] 0.000607072
immunoglobulin m, level of [NCBI] 0.000567689
prognathism, mandibular [NCBI] 0.000536375
ASD1 [NCBI] 0.000510391
GCY [NCBI] 0.000510391
SHOX [NCBI] 0.000472609
XIST [NCBI] 0.000467078
DA5 [NCBI] 0.000451673
gonadal dysgenesis, xy type [NCBI] 0.000436268
ODG1 [NCBI] 0.000370157
LWD [NCBI] 0.000330824
SRY [NCBI] 0.000249327
ISS [NCBI] 0.000243069
nuchal bleb, familial [NCBI] 0.000189726
ODG2 [NCBI] 0.000161791
BDE [NCBI] 0.000161791
aortic valve disease [NCBI] 0.000160745
SHOXY [NCBI] 0.000149428
RA [NCBI] 0.000124134
SHOX2 [NCBI] 0.000121877
POF1 [NCBI] 0.000119364
RPS4X [NCBI] 0.000107824
sjogren-larsson-like ichthyosis without cns or eye involvement [NCBI] 9.47367e-05
SRS [NCBI] 8.68047e-05
genitopalatocardiac syndrome [NCBI] 8.62662e-05
DSS [NCBI] 8.07696e-05
WT1 [NCBI] 7.74856e-05
frasier syndrome [NCBI] 7.34328e-05
HYR [NCBI] 7.07301e-05
MAOA [NCBI] 6.66149e-05
NYS1 [NCBI] 6.6398e-05
WT1 [NCBI] 6.46713e-05
GH1 [NCBI] 6.39455e-05
lymphedema, hereditary, i [NCBI] 6.01878e-05
TPO [NCBI] 5.92733e-05
nondisjunction [NCBI] 5.67342e-05
denys-drash syndrome [NCBI] 5.67342e-05
CDPX1 [NCBI] 5.39002e-05
lymphedema-distichiasis syndrome [NCBI] 5.14985e-05
UCMD [NCBI] 5.00797e-05
faciogenital dysplasia [NCBI] 4.59344e-05
growth hormone insensitivity syndrome [NCBI] 4.26665e-05
FGD1 [NCBI] 4.23842e-05
HEMB [NCBI] 4.14666e-05
campomelic dysplasia [NCBI] 4.06957e-05
SHBG [NCBI] 3.87736e-05
SSX1 [NCBI] 3.82052e-05
BGN [NCBI] 3.75474e-05
GHRH [NCBI] 3.70963e-05
DCN [NCBI] 3.58043e-05
TBG [NCBI] 3.43263e-05
hurler syndrome [NCBI] 3.3952e-05
CHM [NCBI] 3.34528e-05
PAEP [NCBI] 3.05833e-05
DAZ [NCBI] 3.0278e-05
GNRH1 [NCBI] 2.93065e-05
AHO [NCBI] 2.7571e-05
AR [NCBI] 2.62205e-05
KAL1 [NCBI] 2.5994e-05
TG [NCBI] 2.54697e-05
IGFALS [NCBI] 2.164e-05
CD [NCBI] 2.13984e-05
ichthyosis, x-linked [NCBI] 2.11737e-05
PCD [NCBI] 1.97532e-05
DMD [NCBI] 1.8478e-05
VEGF [NCBI] 1.84507e-05
GHR [NCBI] 1.7651e-05
RTT [NCBI] 1.43681e-05
GIP [NCBI] 1.079e-05
CVID [NCBI] 1.03737e-05
AFP [NCBI] 8.41619e-06
TNFRSF11B [NCBI] 4.19194e-06
G6PD [NCBI] 1.47326e-06
PCNA [NCBI] 8.0422e-07
PRL [NCBI] 7.90303e-07



Database Center for Life Science