MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Coronary Vessel Anomalies
[NCBI]
Gene
Gene
Link
Information
Gain
01
ZFPM2
[NCBI]
1.47454e-05
HAND1
[NCBI]
1.35962e-05
TBX1
[NCBI]
1.20826e-05
GATA4
[NCBI]
1.20482e-05
HP
[NCBI]
8.66675e-06
PF4
[NCBI]
8.64328e-06
VEGFA
[NCBI]
5.39762e-06
TNF
[NCBI]
3.36665e-06
OMIM
OMIM
Link
Information
gain
01
splenic hypoplasia
[NCBI]
0.00098052
MVP
[NCBI]
0.000669824
aortic valve disease
[NCBI]
0.000150298
aortic arch interruption, facial palsy, and retinal coloboma
[NCBI]
0.000122684
CMH
[NCBI]
0.000119444
DGS
[NCBI]
0.000113624
ATS
[NCBI]
8.80291e-05
asplenia with cardiovascular anomalies
[NCBI]
8.0832e-05
VEGFB
[NCBI]
7.71931e-05
EFE
[NCBI]
7.25761e-05
ZFPM2
[NCBI]
7.10164e-05
ehlers-danlos syndrome, type i
[NCBI]
7.02662e-05
GATA4
[NCBI]
6.37462e-05
TBX1
[NCBI]
6.17519e-05
velocardiofacial syndrome
[NCBI]
6.03283e-05
SVAS
[NCBI]
5.75747e-05
AVSD
[NCBI]
5.71904e-05
HP
[NCBI]
3.26028e-05
PF4
[NCBI]
3.14811e-05
VEGF
[NCBI]
1.95209e-05
Database Center for Life Science