MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Arnold-Chiari Malformation
[NCBI]
Gene
Gene
Link
Information
Gain
01
AIS
[NCBI]
0.000572277
HFM
[NCBI]
0.000193108
PAX3
[NCBI]
2.03915e-05
GFAP
[NCBI]
1.2732e-05
PAX2
[NCBI]
1.00082e-05
VIM
[NCBI]
9.95259e-06
FGFR2
[NCBI]
9.21896e-06
FGFR3
[NCBI]
7.62409e-06
CFTR
[NCBI]
4.48986e-06
OMIM
OMIM
Link
Information
gain
01
chiari malformation type i
[NCBI]
0.0186857
syringomyelia, isolated
[NCBI]
0.00199086
chiari malformation type ii
[NCBI]
0.000907885
IS1
[NCBI]
0.000372938
NS1
[NCBI]
0.000222768
DWS
[NCBI]
0.000187992
HFM
[NCBI]
0.000100812
papillorenal syndrome
[NCBI]
8.25826e-05
ABS
[NCBI]
7.41402e-05
OKS
[NCBI]
7.41402e-05
autonomic control, congenital failure of
[NCBI]
7.30808e-05
FDH
[NCBI]
6.75057e-05
PAX2
[NCBI]
5.7247e-05
ACADS
[NCBI]
5.68152e-05
PAX3
[NCBI]
4.74319e-05
GFAP
[NCBI]
3.97289e-05
FGFR2
[NCBI]
3.95255e-05
GHRH
[NCBI]
3.45639e-05
CFTR
[NCBI]
1.90616e-05
CJD
[NCBI]
1.75802e-05
CF
[NCBI]
9.9205e-06
RA
[NCBI]
4.73194e-06
Database Center for Life Science