Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Sacrum [NCBI]

Gene


 Gene Link Information
Gain		 01
AIS [NCBI] 0.000565989
MNX1 [NCBI] 0.000163128
FGFR2 [NCBI] 1.64272e-05
MAP7 [NCBI] 7.07209e-06
MIB1 [NCBI] 6.31486e-06
CITED2 [NCBI] 6.16352e-06
BMP2 [NCBI] 6.07067e-06
HOXA11 [NCBI] 5.88894e-06
TNXB [NCBI] 5.24362e-06
ELN [NCBI] 5.06494e-06
AR [NCBI] 4.92097e-06
GFAP [NCBI] 4.24191e-06
CD99 [NCBI] 4.09323e-06
T [NCBI] 3.87001e-06
MYOD1 [NCBI] 3.77646e-06
MMP2 [NCBI] 3.50764e-06
SHH [NCBI] 3.33477e-06
FASLG [NCBI] 1.63148e-06
BDNF [NCBI] 1.62114e-06
NGF [NCBI] 9.7433e-07



OMIM


 OMIM Link Information
gain		 01
currarino syndrome [NCBI] 0.00295346
sacral defect with anterior meningocele [NCBI] 0.00272905
schinzel-giedion midface-retraction syndrome [NCBI] 0.00186478
CHDM [NCBI] 0.00115699
klippel-feil syndrome, autosomal dominant [NCBI] 0.000979436
IS1 [NCBI] 0.000953538
HLXB9 [NCBI] 0.000304352
neural tube defects [NCBI] 0.000263489
chondrodysplasia punctata, brachytelephalangic, autosomal [NCBI] 0.000205148
spondylosis, cervical [NCBI] 0.000165891
velocardiofacial syndrome [NCBI] 0.000157557
spondylolisthesis [NCBI] 0.000151086
vater association [NCBI] 0.000113224
DGS [NCBI] 0.000106923
cerebrocostomandibular syndrome [NCBI] 0.000103342
SGBS1 [NCBI] 8.6672e-05
CES [NCBI] 6.22327e-05
T [NCBI] 4.79875e-05
MFS [NCBI] 4.10148e-05
RA [NCBI] 4.00143e-05
GIST [NCBI] 3.75999e-05
GFAP [NCBI] 1.79393e-05
MUC1 [NCBI] 1.78043e-05
SHH [NCBI] 1.29038e-05
CEACAM5 [NCBI] 8.12248e-06
AR [NCBI] 7.44219e-06
BDNF [NCBI] 5.68822e-06
CRH [NCBI] 5.30692e-06
NGFB [NCBI] 1.92406e-06



Database Center for Life Science