MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
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
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