Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Heart Septal Defects	[NCBI]

Gene	Link	Information Gain
GATA4	[NCBI]	4.90581e-05
CRELD1	[NCBI]	4.48816e-05
NKX2-5	[NCBI]	3.16902e-05
LBH	[NCBI]	1.48774e-05
PPP1R14C	[NCBI]	1.38601e-05
TBX20	[NCBI]	1.29808e-05
FKBP1A	[NCBI]	1.25745e-05
CFC1	[NCBI]	1.19708e-05
HIRA	[NCBI]	1.15252e-05
UFD1L	[NCBI]	1.0879e-05
ACTC1	[NCBI]	1.0879e-05
TBX5	[NCBI]	1.08129e-05
CAV3	[NCBI]	9.45443e-06
ERF	[NCBI]	9.18387e-06
ETS2	[NCBI]	8.86514e-06
NOG	[NCBI]	7.91723e-06
MTR	[NCBI]	7.74715e-06
BMP4	[NCBI]	7.13706e-06
CXCR4	[NCBI]	6.87236e-06
CXCL12	[NCBI]	4.95844e-06
VEGFA	[NCBI]	3.13504e-06

OMIM	Link	Information gain
AVSD	[NCBI]	0.00215647
dandy-walker-like malformation with atrioventricular septal defect	[NCBI]	0.00134416
heterotaxy, visceral, 3, autosomal	[NCBI]	0.000813359
OSCS	[NCBI]	0.000742146
mental retardation, congenital heart disease, blepharophimosis, blepharoptosis, and hypoplastic teeth	[NCBI]	0.000673834
cayler cardiofacial syndrome	[NCBI]	0.000528971
pulmonic stenosis	[NCBI]	0.000200628
GATA4	[NCBI]	0.000135586
ASD4	[NCBI]	0.000127341
HOS	[NCBI]	0.000112823
ASD2	[NCBI]	0.000104875
FKBP1A	[NCBI]	9.57743e-05
heterotaxy, visceral, 2, autosomal	[NCBI]	9.08966e-05
tricuspid atresia	[NCBI]	9.08966e-05
right ventricular hypoplasia, isolated	[NCBI]	8.68069e-05
DFNA10	[NCBI]	8.68069e-05
ATE1	[NCBI]	8.19941e-05
TBX20	[NCBI]	8.19941e-05
acrofacial dysostosis syndrome of rodriguez	[NCBI]	8.08408e-05
DGS	[NCBI]	7.77525e-05
UFD1L	[NCBI]	7.67933e-05
SLOS	[NCBI]	7.16611e-05
MCOPS2	[NCBI]	6.90237e-05
UMS	[NCBI]	6.30979e-05
CXCR4	[NCBI]	5.79776e-05
CAV3	[NCBI]	5.25509e-05
MTR	[NCBI]	4.44535e-05
FBN1	[NCBI]	3.93106e-05
VEGF	[NCBI]	1.76921e-06