Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 [NCBI]

Gene


 Gene Link Information
Gain		 01
VCF [NCBI] 0.000182885
SRY [NCBI] 0.000179305
SOX9 [NCBI] 0.000135489
DMRT1 [NCBI] 5.72729e-05
WNT4 [NCBI] 3.14201e-05
DMRT2 [NCBI] 1.45369e-05
ZFY [NCBI] 1.02103e-05
FOXL2 [NCBI] 8.14936e-06
NR5A1 [NCBI] 7.66849e-06
PRKY [NCBI] 6.71465e-06
PRKX [NCBI] 6.40777e-06
SOX11 [NCBI] 5.8798e-06
SOX1 [NCBI] 5.8798e-06
RBMY1A1 [NCBI] 5.0538e-06
SF1 [NCBI] 4.98331e-06
CYP11A1 [NCBI] 4.93062e-06
FGF9 [NCBI] 4.91791e-06
NR0B1 [NCBI] 4.88082e-06
ATRX [NCBI] 4.68543e-06
KPNB1 [NCBI] 4.45401e-06
TDFA [NCBI] 3.67342e-06
CBX2 [NCBI] 3.2361e-06
RSPO1 [NCBI] 2.97629e-06
DHH [NCBI] 2.78528e-06
SOX17 [NCBI] 2.69168e-06
JARID1D [NCBI] 2.6323e-06
SOX3 [NCBI] 2.21425e-06
AKR1C3 [NCBI] 2.14591e-06
CALM3 [NCBI] 2.13339e-06
NR6A1 [NCBI] 2.11525e-06
GATA4 [NCBI] 2.02917e-06
SOX10 [NCBI] 1.93651e-06
GLI1 [NCBI] 1.90198e-06
CALM1 [NCBI] 1.73693e-06
AMH [NCBI] 1.60885e-06
AR [NCBI] 1.59512e-06
CBX4 [NCBI] 1.43484e-06
STAR [NCBI] 1.42713e-06
DCT [NCBI] 1.42333e-06
SHH [NCBI] 1.21525e-06
PAX6 [NCBI] 9.82931e-07
AVP [NCBI] 5.1742e-07
NPY [NCBI] 4.11368e-07



OMIM


 OMIM Link Information
gain		 01
gonadal dysgenesis, xy type [NCBI] 0.00204613
campomelic dysplasia [NCBI] 0.00163166
pierre robin sequence with pectus excavatum and rib and scapular anomalies [NCBI] 0.00095223
SOX9 [NCBI] 0.000710227
palmoplantar hyperkeratosis with squamous cell carcinoma of skin and sex reversal [NCBI] 0.000704647
FSHMD1A [NCBI] 0.000428904
SRY [NCBI] 0.000407995
meacham syndrome [NCBI] 0.000156274
jejunal atresia with microcephaly and ocular anomalies [NCBI] 0.000156274
spastic paraplegia, optic atrophy, microcephaly, and xy sex reversal [NCBI] 0.000156274
NR0B1 [NCBI] 0.000154495
CYP11A1 [NCBI] 0.000139019
NR5A1 [NCBI] 0.000137823
SERKAL [NCBI] 0.000118034
gonadal dysgenesis, 46,xy, partial, with minifascicular neuropathy [NCBI] 0.000118034
DMRT1 [NCBI] 0.000115175
monosomy 9p syndrome [NCBI] 0.00010618
SRA2 [NCBI] 0.000103395
HYR [NCBI] 9.59433e-05
PMDS [NCBI] 8.74034e-05
lipoid congenital adrenal hyperplasia [NCBI] 8.27812e-05
MCOPS7 [NCBI] 6.86698e-05
NPS [NCBI] 5.96895e-05
FGF9 [NCBI] 5.90264e-05
DHH [NCBI] 5.36057e-05
GDXY [NCBI] 5.14452e-05
PRKY [NCBI] 3.74369e-05
DMRT2 [NCBI] 3.74369e-05
SLOS [NCBI] 3.55588e-05
RSPO1 [NCBI] 3.54169e-05
neuroblastoma stage 4s gene [NCBI] 3.39153e-05
INSRR [NCBI] 3.39153e-05
CBX2 [NCBI] 3.27189e-05
WNT4 [NCBI] 2.94683e-05
AMH [NCBI] 2.75903e-05
JARID1D [NCBI] 2.65638e-05
IGF1R [NCBI] 2.21856e-05
ESR2 [NCBI] 2.11873e-05
ATRX [NCBI] 1.99521e-05
DCT [NCBI] 1.98297e-05
WT1 [NCBI] 1.83436e-05
ESR1 [NCBI] 1.45318e-05
INSR [NCBI] 1.37742e-05
STAR [NCBI] 8.91889e-06
AR [NCBI] 4.68826e-06
GNRH1 [NCBI] 4.13343e-06
SHH [NCBI] 3.51357e-06
NPY [NCBI] 8.61938e-08
AVP [NCBI] 7.6648e-09



Database Center for Life Science