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01 Urogenital Abnormalities [NCBI]

Gene


 Gene Link Information
Gain		 01
VUR [NCBI] 0.000766829
POM121L1 [NCBI] 0.000373825
EEC2 [NCBI] 0.000373825
FGD1 [NCBI] 0.000133207
HOXA13 [NCBI] 0.000113693
WT1 [NCBI] 4.31337e-05
HOXD13 [NCBI] 4.08534e-05
PAX2 [NCBI] 2.48933e-05
CFTR [NCBI] 1.84897e-05
WNT4 [NCBI] 1.83324e-05
ARX [NCBI] 1.74551e-05
ATRX [NCBI] 1.74551e-05
FAM58A [NCBI] 1.39434e-05
FGD2 [NCBI] 1.3045e-05
NKX3-2 [NCBI] 1.3045e-05
RCN1 [NCBI] 1.24616e-05
FGD3 [NCBI] 1.24616e-05
FRAS1 [NCBI] 1.20279e-05
SHH [NCBI] 1.17258e-05
DBNL [NCBI] 1.16822e-05
NFIA [NCBI] 1.16822e-05
HOXA3 [NCBI] 1.16822e-05
UPK3A [NCBI] 1.04146e-05
HAX1 [NCBI] 9.34103e-06
MED12 [NCBI] 9.26307e-06
COL9A3 [NCBI] 9.18852e-06
MKKS [NCBI] 8.91907e-06
BBS1 [NCBI] 8.74164e-06
SALL1 [NCBI] 8.434e-06
MDK [NCBI] 8.09469e-06
GLI2 [NCBI] 7.91247e-06
TGFA [NCBI] 7.65622e-06
NSD1 [NCBI] 7.43354e-06
IRF6 [NCBI] 7.35702e-06
FGF8 [NCBI] 7.28379e-06
CTTN [NCBI] 7.10268e-06
AXIN1 [NCBI] 6.7371e-06
AMH [NCBI] 6.1447e-06
BMP4 [NCBI] 5.32345e-06
PAX6 [NCBI] 4.85297e-06
KRT7 [NCBI] 4.43042e-06
KRT20 [NCBI] 4.06419e-06
CST3 [NCBI] 3.21625e-06
CAT [NCBI] 2.58056e-06
EGF [NCBI] 7.77016e-07



OMIM


 OMIM Link Information
gain		 01
urogenital adysplasia, hereditary [NCBI] 0.00188374
pubic bone dysplasia [NCBI] 0.000984578
abdominal muscles, absence of, with urinary tract abnormality and cryptorchidism [NCBI] 0.000813264
EEC1 [NCBI] 0.000782158
trichoscyphodysplasia [NCBI] 0.000766909
genitopatellar syndrome [NCBI] 0.0006318
exstrophy of bladder [NCBI] 0.000592366
IH [NCBI] 0.000446614
MRD [NCBI] 0.000391288
WT1 [NCBI] 0.000389164
cayler cardiofacial syndrome [NCBI] 0.000351123
FGD1 [NCBI] 0.000340438
VUR1 [NCBI] 0.00033146
chiari malformation type i [NCBI] 0.000325462
hand-foot-uterus syndrome [NCBI] 0.000318393
WT1 [NCBI] 0.000304857
thrombocytopenia-absent radius syndrome [NCBI] 0.00029877
frasier syndrome [NCBI] 0.000272844
oeis complex [NCBI] 0.000254496
b-cell immunodeficiency, distal limb anomalies, and urogenital malformations [NCBI] 0.000226613
hypertelorism with esophageal abnormality and hypospadias [NCBI] 0.000222553
kabuki syndrome [NCBI] 0.000217149
denys-drash syndrome [NCBI] 0.000215242
GUD [NCBI] 0.000195673
spondylocostal dysostosis with anal atresia and urogenital anomalies [NCBI] 0.000195673
faciogenital dysplasia [NCBI] 0.000180854
malpuech facial clefting syndrome [NCBI] 0.000172108
AN2 [NCBI] 0.000155961
rokitansky-kuster-hauser syndrome [NCBI] 0.000153775
SLOS [NCBI] 0.000132762
papillorenal syndrome [NCBI] 0.000125063
prune belly syndrome with pulmonic stenosis, mental retardation, and deafness [NCBI] 0.000113208
nephrosis with deafness and urinary tract and digital malformations [NCBI] 0.000113208
HOXA13 [NCBI] 0.000111138
ATRX [NCBI] 0.000109036
ABS [NCBI] 0.000107912
MKKS [NCBI] 0.000106828
SRS [NCBI] 0.000105256
TBS [NCBI] 0.000101003
caudal duplication anomaly [NCBI] 9.075e-05
VUR2 [NCBI] 9.075e-05
ATRX [NCBI] 8.41263e-05
KPC [NCBI] 8.22828e-05
acrofrontofacionasal dysostosis, severe [NCBI] 8.22828e-05
FGD2 [NCBI] 8.13558e-05
pulmonary hypertension, familial persistent, of the newborn [NCBI] 7.27084e-05
cleft larynx, posterior [NCBI] 6.94592e-05
AXIN1 [NCBI] 6.75778e-05
antigen defined by monoclonal antibody f10.44.2 [NCBI] 6.75778e-05
RCN1 [NCBI] 6.75778e-05
NEGF2 [NCBI] 6.75778e-05
gastroschisis [NCBI] 6.4451e-05
corpus callosum, agenesis of [NCBI] 6.24343e-05
NFIA [NCBI] 6.23791e-05
BBS [NCBI] 6.14716e-05
WNT4 [NCBI] 5.6495e-05
hydrocephalus [NCBI] 5.62372e-05
LDS [NCBI] 5.62372e-05
lymphedema, hereditary, i [NCBI] 5.62372e-05
disorganization, mouse, homolog of [NCBI] 5.62372e-05
currarino syndrome [NCBI] 5.50039e-05
EMX2 [NCBI] 5.44961e-05
multiple pterygium syndrome, escobar variant [NCBI] 5.386e-05
EEC3 [NCBI] 5.17945e-05
sacral defect with anterior meningocele [NCBI] 5.08554e-05
MKKS [NCBI] 5.0169e-05
FSHB [NCBI] 5.0169e-05
RTD [NCBI] 4.83347e-05
SALL1 [NCBI] 4.71697e-05
BGS [NCBI] 4.55045e-05
PAX8 [NCBI] 4.48725e-05
MRXHF1 [NCBI] 4.48709e-05
donohue syndrome [NCBI] 4.42622e-05
HOXD13 [NCBI] 4.4212e-05
LRP2 [NCBI] 4.4212e-05
IRF6 [NCBI] 4.35931e-05
CFTR [NCBI] 4.16987e-05
fraser syndrome [NCBI] 4.15347e-05
PAX2 [NCBI] 4.05257e-05
TP73L [NCBI] 3.96845e-05
TGFBR2 [NCBI] 3.92895e-05
apert syndrome [NCBI] 3.92211e-05
XPA [NCBI] 3.6128e-05
ARPKD [NCBI] 3.13879e-05
PAX6 [NCBI] 3.11252e-05
CF [NCBI] 3.0105e-05
velocardiofacial syndrome [NCBI] 2.92743e-05
NS1 [NCBI] 2.42053e-05
AMH [NCBI] 2.23062e-05
CDLS1 [NCBI] 2.16034e-05
CAT [NCBI] 1.9856e-05
BCNS [NCBI] 1.62379e-05
DGS [NCBI] 1.53891e-05
AT [NCBI] 7.94033e-06
MUC1 [NCBI] 7.69229e-06
FA [NCBI] 2.58197e-06
EGF [NCBI] 1.92655e-07



Database Center for Life Science