Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Heart Septum	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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