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MeSH keywords -> Related genes, diseases (OMIM)


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01 Heart Septum [NCBI]

Gene


 Gene Link Information
Gain		 01
HAND1 [NCBI] 1.25544e-05
STARD10 [NCBI] 8.27208e-06
LBH [NCBI] 7.63384e-06
MYBPC1 [NCBI] 7.24743e-06
HEY2 [NCBI] 7.09879e-06
HIRA [NCBI] 6.17469e-06
HAND2 [NCBI] 6.02241e-06
ATP1A1 [NCBI] 5.75544e-06
NPPB [NCBI] 5.72003e-06
HCN4 [NCBI] 5.58976e-06
NOTCH4 [NCBI] 5.13241e-06
FBLN1 [NCBI] 5.0315e-06
KCNA5 [NCBI] 4.96404e-06
NPPA [NCBI] 4.90086e-06
PIH [NCBI] 4.56612e-06
TGFBI [NCBI] 4.39576e-06
MB [NCBI] 4.3596e-06
NPY [NCBI] 4.29508e-06
ACE [NCBI] 4.17391e-06
KCNJ8 [NCBI] 4.11323e-06
JAG1 [NCBI] 3.74239e-06
NOTCH1 [NCBI] 3.72588e-06
SNAI2 [NCBI] 3.7005e-06
SPI1 [NCBI] 3.4791e-06
NOG [NCBI] 3.39717e-06
TGFBR1 [NCBI] 3.34508e-06
TNF [NCBI] 2.81478e-06
BMP2 [NCBI] 2.59721e-06
AFP [NCBI] 2.55725e-06
VWF [NCBI] 2.27206e-06
VEGFA [NCBI] 2.05558e-06
BAX [NCBI] 1.96918e-06
TH [NCBI] 1.58229e-06
NGF [NCBI] 1.1959e-06



OMIM


 OMIM Link Information
gain		 01
CMH [NCBI] 0.00580556
aneurysm of interventricular septum [NCBI] 0.000390242
AVSD [NCBI] 0.000264263
pulmonary atresia with intact ventricular septum [NCBI] 0.000194849
marfanoid hypermobility syndrome [NCBI] 0.000140805
atrial septal defect with atrioventricular conduction defects [NCBI] 0.000124076
heart block, congenital [NCBI] 0.0001184
CMD1A [NCBI] 7.77385e-05
ehlers-danlos syndrome, type i [NCBI] 7.65866e-05
HEY2 [NCBI] 5.30409e-05
BBS [NCBI] 4.45036e-05
CF [NCBI] 4.07838e-05
PXE [NCBI] 3.04643e-05
SLE [NCBI] 2.89582e-05
MB [NCBI] 2.6674e-05
DGS [NCBI] 2.62681e-05
NPY [NCBI] 2.20703e-05
AFP [NCBI] 1.37344e-05
TNF [NCBI] 1.31459e-05
TH [NCBI] 6.9488e-06
NGFB [NCBI] 4.47594e-06
VEGF [NCBI] 2.97338e-06



Database Center for Life Science