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MeSH keywords -> Related genes, diseases (OMIM)


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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