Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 [NCBI]


Gene


Gene Link Information
Gain
01
ACTGP10 [NCBI] 0.000499621
SRY [NCBI] 0.000331416
ZFY [NCBI] 9.90881e-05
WNT4 [NCBI] 2.96807e-05
AMH [NCBI] 2.41783e-05
SOX9 [NCBI] 2.40321e-05
SOX1 [NCBI] 2.37204e-05
FOXL2 [NCBI] 1.79927e-05
AR [NCBI] 1.5552e-05
NCAPH [NCBI] 1.39434e-05
TDFA [NCBI] 1.39434e-05
CST9L [NCBI] 1.3045e-05
SMC2 [NCBI] 1.24616e-05
MAMLD1 [NCBI] 1.16822e-05
PKD1 [NCBI] 1.0644e-05
HMCN1 [NCBI] 1.02715e-05
DDX6 [NCBI] 1.02715e-05
RRAS [NCBI] 1.00167e-05
CUL2 [NCBI] 9.11707e-06
FGF9 [NCBI] 9.04849e-06
DMRT1 [NCBI] 8.85786e-06
RBMY1A1 [NCBI] 8.25593e-06
TSPY1 [NCBI] 8.01945e-06
SRD5A2 [NCBI] 6.60402e-06
DAZ1 [NCBI] 6.4079e-06
CYP21A2 [NCBI] 6.09666e-06
ERG [NCBI] 5.05558e-06
SHBG [NCBI] 3.62449e-06
EGF [NCBI] 7.77016e-07




OMIM


OMIM Link Information
gain
01
AIS [NCBI] 0.00157721
pseudohermaphroditism, female, with skeletal anomalies [NCBI] 0.00137383
hermaphroditism, true [NCBI] 0.00122708
trichoscyphodysplasia [NCBI] 0.00115589
pseudohermaphroditism, incomplete male, type i [NCBI] 0.000424736
SRA2 [NCBI] 0.000423313
SRY [NCBI] 0.000359948
palmoplantar hyperkeratosis with squamous cell carcinoma of skin and sex reversal [NCBI] 0.000174809
reifenstein syndrome [NCBI] 0.000165434
17-@beta hydroxysteroid dehydrogenase iii deficiency [NCBI] 0.000147287
GDXY [NCBI] 0.000147211
denys-drash syndrome [NCBI] 0.000145055
PPSH [NCBI] 0.000121644
AMH [NCBI] 0.000102966
myotubular myopathy with abnormal genital development [NCBI] 9.02278e-05
hypogonadism, male [NCBI] 8.47286e-05
gracile bone dysplasia [NCBI] 7.73868e-05
AR [NCBI] 7.66824e-05
GULP1 [NCBI] 6.86113e-05
B3GALT5 [NCBI] 6.86113e-05
FGF9 [NCBI] 6.34123e-05
lipoid congenital adrenal hyperplasia [NCBI] 6.06627e-05
CXORF6 [NCBI] 6.0037e-05
SLOS [NCBI] 5.97942e-05
adrenal hyperplasia, congenital, due to 17-alpha-hydroxylase deficiency [NCBI] 5.69765e-05
HMCN1 [NCBI] 5.55285e-05
JBS [NCBI] 5.39878e-05
ATRX [NCBI] 5.09058e-05
ACTA1 [NCBI] 5.00962e-05
RAC1 [NCBI] 4.82005e-05
3-@beta-hydroxysteroid dehydrogenase, type ii, deficiency of [NCBI] 4.66106e-05
spermatogenic failure, nonobstructive, y-linked [NCBI] 4.53184e-05
FOXL2 [NCBI] 4.34898e-05
BPES [NCBI] 4.03473e-05
MTM1 [NCBI] 4.03473e-05
NR5A1 [NCBI] 4.03164e-05
WT1 [NCBI] 3.30189e-05
WT1 [NCBI] 3.15959e-05
LRP1 [NCBI] 2.50329e-05
TP53 [NCBI] 1.9184e-05
SHBG [NCBI] 1.00437e-05
EGF [NCBI] 3.83853e-08




Database Center for Life Science