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MeSH keywords -> Related genes, diseases (OMIM)


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01 Pelvis [NCBI]

Gene


 Gene Link Information
Gain		 01
AIS [NCBI] 0.00194076
KTWS [NCBI] 0.000240473
TH [NCBI] 3.27325e-05
VIP [NCBI] 3.08935e-05
NPY [NCBI] 2.3943e-05
PITX1 [NCBI] 2.0158e-05
MNX1 [NCBI] 1.82405e-05
F8 [NCBI] 9.07542e-06
PDAP1 [NCBI] 7.26373e-06
LARP7 [NCBI] 7.06216e-06
CHAT [NCBI] 6.67451e-06
DYM [NCBI] 6.62563e-06
ZNF384 [NCBI] 6.32286e-06
SGCD [NCBI] 6.02406e-06
CCK [NCBI] 5.75463e-06
TNFRSF11B [NCBI] 5.75176e-06
LOXL1 [NCBI] 5.56603e-06
LTBP2 [NCBI] 5.48756e-06
GALNS [NCBI] 5.25323e-06
HOXA11 [NCBI] 5.14051e-06
SLC26A2 [NCBI] 4.92562e-06
NRTN [NCBI] 4.7856e-06
UPK2 [NCBI] 4.56854e-06
LTBP1 [NCBI] 4.53898e-06
HOXA10 [NCBI] 4.52452e-06
LOX [NCBI] 4.37803e-06
SLC18A3 [NCBI] 4.36573e-06
COL3A1 [NCBI] 4.14713e-06
PAX1 [NCBI] 4.07162e-06
GNAS [NCBI] 3.75553e-06
COL1A1 [NCBI] 3.63757e-06
FGF23 [NCBI] 3.59746e-06
PLAU [NCBI] 3.51664e-06
HGF [NCBI] 3.51389e-06
AR [NCBI] 3.48178e-06
MPO [NCBI] 3.45712e-06
FOLH1 [NCBI] 3.35935e-06
LEP [NCBI] 3.05554e-06
PGR [NCBI] 2.97822e-06
MATN1 [NCBI] 2.89023e-06
FGFR3 [NCBI] 2.87143e-06
MMP13 [NCBI] 2.85561e-06
UMOD [NCBI] 2.77535e-06
MMP2 [NCBI] 2.77055e-06
MAPK3 [NCBI] 2.74458e-06
H2AFX [NCBI] 2.67715e-06
CXCR4 [NCBI] 2.62029e-06
BCL2 [NCBI] 2.57832e-06
EGF [NCBI] 2.48976e-06
PRL [NCBI] 2.43706e-06
TGFBR1 [NCBI] 2.35954e-06
SLC2A1 [NCBI] 2.32609e-06
CAV1 [NCBI] 2.30541e-06
GAPDH [NCBI] 2.24055e-06
MAPK1 [NCBI] 2.23647e-06
PTHLH [NCBI] 2.22435e-06
TNFRSF11A [NCBI] 2.13883e-06
PTGS1 [NCBI] 2.09134e-06
TNFSF11 [NCBI] 2.01804e-06
PLAUR [NCBI] 1.74384e-06
CXCL12 [NCBI] 1.70557e-06
HRAS [NCBI] 1.68412e-06
AFP [NCBI] 1.60002e-06
LIF [NCBI] 1.4915e-06
TP53 [NCBI] 1.19903e-06
TGFB1 [NCBI] 1.09875e-06
AKT1 [NCBI] 1.02115e-06
PCNA [NCBI] 1.00764e-06
PTGS2 [NCBI] 7.96307e-07
ACHE [NCBI] 7.86372e-07
PTH [NCBI] 7.20124e-07
CDKN1A [NCBI] 7.01301e-07
NGF [NCBI] 4.07439e-07
MS [NCBI] 5.20847e-08



OMIM


 OMIM Link Information
gain		 01
IS1 [NCBI] 0.00424832
pelvic organ prolapse [NCBI] 0.000990474
ATD1 [NCBI] 0.000968064
spondylometaphyseal dysplasia, corner fracture type [NCBI] 0.000873756
LGMD1D [NCBI] 0.000873756
oculodentoosseous dysplasia, recessive [NCBI] 0.000798192
epiphyseal dysplasia, microcephaly, and nystagmus [NCBI] 0.000742173
microcephalic osteodysplastic primordial dwarfism, type ii [NCBI] 0.000697666
KLK3 [NCBI] 0.000624252
kyphomelic dysplasia [NCBI] 0.000601823
ACG1A [NCBI] 0.000555704
OSCS [NCBI] 0.000535946
pelvis-shoulder dysplasia [NCBI] 0.000522489
DMC [NCBI] 0.000395252
currarino syndrome [NCBI] 0.000380402
melorheostosis [NCBI] 0.000336168
klippel-trenaunay-weber syndrome [NCBI] 0.000299007
schneckenbecken dysplasia [NCBI] 0.000294987
buschke-ollendorff syndrome [NCBI] 0.000248692
EDMD2 [NCBI] 0.000223729
PPAC [NCBI] 0.000216208
LGMD2A [NCBI] 0.000200925
chondrosarcoma [NCBI] 0.000194849
syndesmodysplasic dwarfism [NCBI] 0.000194849
dwarfism with tall vertebrae [NCBI] 0.000194849
pelviscapular dysplasia [NCBI] 0.000194849
syndactyly with renal and anogenital malformations [NCBI] 0.000194849
pelvic hypoplasia with lower-limb arthrogryposis [NCBI] 0.000155601
dysplasia epiphysealis hemimelica [NCBI] 0.000155601
spondylometaphyseal dysplasia, east african type [NCBI] 0.000155601
EDM5 [NCBI] 0.000155601
platyspondyly with amelogenesis imperfecta [NCBI] 0.000155601
thoracopelvic dysostosis [NCBI] 0.000155601
roifman syndrome [NCBI] 0.000155601
TD1 [NCBI] 0.000151481
LGMD2F [NCBI] 0.000131206
TLPD [NCBI] 0.000131206
LAM [NCBI] 0.000130307
EDM4 [NCBI] 0.000124076
SMC [NCBI] 0.000124076
SPS [NCBI] 0.0001184
fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly [NCBI] 0.0001184
LGMD2E [NCBI] 0.000113685
three m syndrome [NCBI] 0.000109653
morquio syndrome b [NCBI] 0.000106131
immunoosseous dysplasia, schimke type [NCBI] 0.000106131
spondyloepimetaphyseal dysplasia, strudwick type [NCBI] 0.000103005
exostoses, multiple, type ii [NCBI] 0.000100196
mucolipidosis iiia [NCBI] 8.59189e-05
HCH [NCBI] 8.29101e-05
HAE [NCBI] 8.29101e-05
SEDC [NCBI] 8.29101e-05
MNS [NCBI] 8.29101e-05
TRPS1 [NCBI] 7.89418e-05
VIP [NCBI] 7.74738e-05
TH [NCBI] 7.72212e-05
MSD [NCBI] 7.05533e-05
MAS [NCBI] 4.99112e-05
ACH [NCBI] 4.9117e-05
ACPP [NCBI] 4.70797e-05
NPY [NCBI] 4.63374e-05
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiency [NCBI] 4.41828e-05
BCNS [NCBI] 4.32456e-05
GAL [NCBI] 3.69896e-05
KSS [NCBI] 3.68585e-05
LOXL1 [NCBI] 3.42797e-05
SGCD [NCBI] 3.32509e-05
WNT7A [NCBI] 3.23518e-05
HLXB9 [NCBI] 3.23518e-05
DMD [NCBI] 3.20787e-05
SLC26A2 [NCBI] 3.15534e-05
EXT2 [NCBI] 3.01834e-05
ACCN3 [NCBI] 3.01834e-05
PITX1 [NCBI] 2.95861e-05
GIST [NCBI] 2.8648e-05
EXT1 [NCBI] 2.85237e-05
MMP13 [NCBI] 2.85237e-05
NRTN [NCBI] 2.53866e-05
COL1A1 [NCBI] 1.86303e-05
lymphoma, non-hodgkin, familial [NCBI] 1.84093e-05
LOX [NCBI] 1.82806e-05
BMP2 [NCBI] 1.70388e-05
TNFRSF11B [NCBI] 1.34449e-05
FGFR3 [NCBI] 1.20145e-05
RNASE3 [NCBI] 1.1817e-05
SLC18A3 [NCBI] 1.03861e-05
PGR [NCBI] 1.00635e-05
CHAT [NCBI] 8.6708e-06
NGFB [NCBI] 6.14631e-06
APC [NCBI] 5.6489e-06
CCK [NCBI] 4.57e-06
EGF [NCBI] 3.34156e-06
GAPDH [NCBI] 3.29193e-06
AR [NCBI] 2.64091e-06
HGF [NCBI] 2.17422e-06
PTH [NCBI] 1.73414e-06
MPO [NCBI] 1.7009e-06
GDNF [NCBI] 1.60324e-06
ACHE [NCBI] 1.29353e-06
AVP [NCBI] 7.70566e-07
CRH [NCBI] 6.25827e-07
AFP [NCBI] 5.27027e-07
NPPA [NCBI] 3.17349e-07
PCNA [NCBI] 2.50731e-07
CEACAM5 [NCBI] 2.54211e-08
VEGF [NCBI] 1.38219e-08
PRL [NCBI] 9.1294e-09



Database Center for Life Science