Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Sacrum	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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