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MeSH keywords -> Related genes, diseases (OMIM)


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01 Mullerian Ducts [NCBI]


Gene


Gene Link Information
Gain
01
AMH [NCBI] 0.000459285
AMHR2 [NCBI] 6.46955e-05
WNT4 [NCBI] 5.70157e-05
TP63 [NCBI] 2.02394e-05
WNT7A [NCBI] 1.77705e-05
SRY [NCBI] 1.66339e-05
SF3A2 [NCBI] 1.2285e-05
BMPR1B [NCBI] 1.01551e-05
SMAD5 [NCBI] 9.51274e-06
ZFY [NCBI] 9.16975e-06
DMRT1 [NCBI] 8.70387e-06
KRT7 [NCBI] 7.29243e-06
KRT20 [NCBI] 7.01968e-06
SOX9 [NCBI] 6.83745e-06
BBS7 [NCBI] 6.56982e-06
KLHL4 [NCBI] 6.56982e-06
BBS2 [NCBI] 6.18954e-06
WFDC2 [NCBI] 5.99825e-06
MKKS [NCBI] 5.83776e-06
BBS4 [NCBI] 5.69953e-06
BBS1 [NCBI] 5.52256e-06
AR [NCBI] 5.45804e-06
TBX5 [NCBI] 5.4199e-06
DEFB126 [NCBI] 5.37228e-06
LHX1 [NCBI] 5.24171e-06
HOXA7 [NCBI] 5.05612e-06
PCSK5 [NCBI] 5.02282e-06
TBX3 [NCBI] 4.99059e-06
EGF [NCBI] 4.93986e-06
HOXA11 [NCBI] 4.81647e-06
GHSR [NCBI] 4.58056e-06
TSPY1 [NCBI] 4.2012e-06
HOXA10 [NCBI] 4.2012e-06
NR5A1 [NCBI] 4.11876e-06
PAH [NCBI] 3.56012e-06
WNT5A [NCBI] 3.48114e-06
PAX2 [NCBI] 3.36425e-06
CYP19A1 [NCBI] 3.33412e-06
RBL1 [NCBI] 3.3282e-06
RBL2 [NCBI] 3.18071e-06
CD99 [NCBI] 3.03075e-06
CKAP4 [NCBI] 2.95161e-06
HNF1B [NCBI] 2.61464e-06
GJB2 [NCBI] 2.30805e-06
EGFR [NCBI] 2.21154e-06
TGFBR1 [NCBI] 2.04854e-06
ESR1 [NCBI] 1.9194e-06
AHR [NCBI] 1.7569e-06
VDR [NCBI] 1.62755e-06
CTNNB1 [NCBI] 1.00794e-06
PRL [NCBI] 4.13524e-07
NGF [NCBI] 2.15436e-07




OMIM


OMIM Link Information
gain
01
mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly [NCBI] 0.00533036
AMH [NCBI] 0.00318785
PMDS [NCBI] 0.00208822
murcs association [NCBI] 0.000665174
urogenital adysplasia, hereditary [NCBI] 0.000615709
hand-foot-uterus syndrome [NCBI] 0.000433003
AIS [NCBI] 0.000224573
hypomelia with mullerian duct anomalies [NCBI] 0.000204382
renal and mullerian duct hypoplasia [NCBI] 0.000204382
vitamin d-dependent rickets, type ii [NCBI] 0.000203876
SERKAL [NCBI] 0.000165126
mullerian aplasia [NCBI] 0.000150321
uterine anomalies [NCBI] 0.000150321
BBS [NCBI] 0.00014542
AMHR2 [NCBI] 0.000139919
MLRD [NCBI] 0.000133576
TRS [NCBI] 0.000119128
hermaphroditism, true [NCBI] 0.000119128
NR5A1 [NCBI] 0.000113867
rokitansky-kuster-hauser syndrome [NCBI] 0.000112463
ulna and fibula, absence of, with severe limb deficiency [NCBI] 0.000109646
MKKS [NCBI] 8.95592e-05
PHS [NCBI] 8.07602e-05
WNT4 [NCBI] 7.50513e-05
HOXA10 [NCBI] 7.33505e-05
SRY [NCBI] 7.22873e-05
hypogonadotropic hypogonadism [NCBI] 7.13368e-05
BCNS [NCBI] 5.20768e-05
SF3A2 [NCBI] 4.46639e-05
WNT9B [NCBI] 4.46639e-05
SLOS [NCBI] 4.36384e-05
HOXA11 [NCBI] 4.08993e-05
MUC1 [NCBI] 3.62662e-05
HOXA9 [NCBI] 3.51933e-05
FSHB [NCBI] 3.29623e-05
WNT7A [NCBI] 3.20634e-05
BMPR1A [NCBI] 3.12652e-05
HOXA7 [NCBI] 3.05474e-05
PG [NCBI] 1.67597e-05
KITLG [NCBI] 1.113e-05
VDR [NCBI] 1.02267e-05
ACPP [NCBI] 8.06912e-06
NGFB [NCBI] 6.7219e-06
KLK3 [NCBI] 4.84406e-06
PRL [NCBI] 2.84087e-06
AR [NCBI] 2.36171e-06
AHR [NCBI] 2.26805e-06
EGFR [NCBI] 5.83057e-07
EGF [NCBI] 1.49199e-08




Database Center for Life Science