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MeSH keywords -> Related genes, diseases (OMIM)


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01 Gonadal Dysgenesis [NCBI]


Gene


Gene Link Information
Gain
01
PUJO [NCBI] 0.000415947
SRY [NCBI] 0.000307737
ZFY [NCBI] 6.91008e-05
AMH [NCBI] 4.34439e-05
TSPY1 [NCBI] 4.08389e-05
TSPYL1 [NCBI] 2.88354e-05
WNT4 [NCBI] 2.88339e-05
DHH [NCBI] 2.43901e-05
SOX9 [NCBI] 2.31874e-05
WT1 [NCBI] 2.22975e-05
INSL3 [NCBI] 1.53989e-05
POU5F1 [NCBI] 1.50601e-05
FOXD2 [NCBI] 1.3665e-05
LHX9 [NCBI] 1.3665e-05
CST9L [NCBI] 1.27666e-05
ACD [NCBI] 1.1404e-05
MAGEB1 [NCBI] 1.06555e-05
ZFPM2 [NCBI] 1.02926e-05
SMARCA1 [NCBI] 9.73865e-06
RXFP2 [NCBI] 9.2305e-06
SAT1 [NCBI] 9.2305e-06
NR5A1 [NCBI] 8.52102e-06
TFAP2C [NCBI] 8.46392e-06
SALL1 [NCBI] 8.15642e-06
SMARCA2 [NCBI] 8.0651e-06
RBMY1A1 [NCBI] 7.97843e-06
AGA [NCBI] 7.89596e-06
FSHR [NCBI] 7.37911e-06
PBX1 [NCBI] 7.34965e-06
SMARCA4 [NCBI] 6.89167e-06
GLI3 [NCBI] 6.72207e-06
SHOX [NCBI] 6.06254e-06
SAT2 [NCBI] 5.38692e-06
AR [NCBI] 4.96719e-06
TPO [NCBI] 4.09324e-06
TP63 [NCBI] 3.97398e-06
SHBG [NCBI] 3.3602e-06
FMR1 [NCBI] 2.9422e-06
TRH [NCBI] 2.57771e-06
TG [NCBI] 2.50771e-06
PRL [NCBI] 1.19261e-06
PCNA [NCBI] 1.16498e-06




OMIM


OMIM Link Information
gain
01
gonadal dysgenesis, xx type, with deafness [NCBI] 0.00229642
gonadal dysgenesis, xy type [NCBI] 0.00218402
GBY [NCBI] 0.00151576
GCY [NCBI] 0.000600386
ODG1 [NCBI] 0.000538959
kenny-caffey syndrome, type 2 [NCBI] 0.000525644
GDXY [NCBI] 0.000463736
MRD [NCBI] 0.000455679
PCD [NCBI] 0.000372002
frasier syndrome [NCBI] 0.000314637
WT1 [NCBI] 0.000297487
TRS [NCBI] 0.000289208
SRY [NCBI] 0.000283968
SIDDT [NCBI] 0.000254219
AMH [NCBI] 0.000236215
gonadal agenesis [NCBI] 0.000209286
campomelic dysplasia [NCBI] 0.000205896
WT1 [NCBI] 0.000165181
LHX9 [NCBI] 0.000160618
denys-drash syndrome [NCBI] 0.000156583
gonadal dysgenesis, hypergonadotropic, xx type, short stature, and recurrent metabolic acidosis [NCBI] 0.000126878
gonadal dysgenesis, xy type, with associated anomalies [NCBI] 0.000126878
DSS [NCBI] 9.0434e-05
gonadal dysgenesis, 46,xy, partial, with minifascicular neuropathy [NCBI] 9.0434e-05
cardiomyopathy, congestive, with hypergonadotropic hypogonadism [NCBI] 9.0434e-05
FSHR [NCBI] 8.63386e-05
ACD [NCBI] 8.01986e-05
TSPYL1 [NCBI] 8.01986e-05
SMARCA2 [NCBI] 8.01986e-05
polydactyly, postaxial, type a1 [NCBI] 7.80613e-05
AIS [NCBI] 7.75449e-05
KFSD [NCBI] 6.34853e-05
SAT1 [NCBI] 6.12225e-05
VWM [NCBI] 5.83269e-05
GLI2 [NCBI] 5.78478e-05
SMOH [NCBI] 5.78478e-05
fraser syndrome [NCBI] 5.49394e-05
GLI [NCBI] 5.16791e-05
PHS [NCBI] 4.97833e-05
GCPS [NCBI] 4.94212e-05
SRA2 [NCBI] 4.69181e-05
DHH [NCBI] 4.60162e-05
aortic valve disease [NCBI] 4.50762e-05
PTCH1 [NCBI] 3.98249e-05
GLI3 [NCBI] 3.89467e-05
NR5A1 [NCBI] 3.81408e-05
SOX9 [NCBI] 3.73963e-05
NS1 [NCBI] 3.70442e-05
aspartylglucosaminuria [NCBI] 3.63762e-05
SHOX [NCBI] 3.46093e-05
SLOS [NCBI] 2.46012e-05
BGLAP [NCBI] 2.28381e-05
TPO [NCBI] 1.46188e-05
GNRH1 [NCBI] 1.33749e-05
AR [NCBI] 1.1e-05
SHBG [NCBI] 8.23637e-06
TG [NCBI] 4.37431e-06
PCNA [NCBI] 1.5375e-07
PRL [NCBI] 1.12575e-07




Database Center for Life Science