Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Atrioventricular Node	[NCBI]

Gene	Link	Information Gain
NKX2-5	[NCBI]	2.30266e-05
TROVE2	[NCBI]	2.13981e-05
ACHE	[NCBI]	1.99162e-05
HCN4	[NCBI]	1.97439e-05
NPY	[NCBI]	1.46533e-05
TH	[NCBI]	1.12126e-05
SCN5A	[NCBI]	1.02471e-05
VIP	[NCBI]	8.15922e-06
KCNK17	[NCBI]	7.91847e-06
GJA5	[NCBI]	6.10861e-06
ACTN2	[NCBI]	5.60361e-06
RYR2	[NCBI]	5.43796e-06
MYOM2	[NCBI]	4.88864e-06
GJA1	[NCBI]	4.44243e-06
KCNQ1	[NCBI]	4.21727e-06
NR3C1	[NCBI]	3.93156e-06
COMT	[NCBI]	3.36973e-06
BMP4	[NCBI]	3.30036e-06
NOG	[NCBI]	3.24721e-06
BMP2	[NCBI]	2.44984e-06
NOS2	[NCBI]	2.12603e-06
TGFB1	[NCBI]	1.87382e-06
PCNA	[NCBI]	1.77352e-06

OMIM	Link	Information gain
atrioventricular conduction time	[NCBI]	0.000410547
atrial septal defect with atrioventricular conduction defects	[NCBI]	0.000369323
ebstein anomaly	[NCBI]	0.000167602
heart block, congenital	[NCBI]	0.000154754
PFHB1A	[NCBI]	0.000133873
hyperoxaluria, primary, type i	[NCBI]	0.000117558
SLE	[NCBI]	0.00010078
AVSD	[NCBI]	9.22466e-05
NKX2E	[NCBI]	8.46451e-05
ACHE	[NCBI]	7.98627e-05
KCNK17	[NCBI]	5.51981e-05
NPY	[NCBI]	5.28038e-05
GJD3	[NCBI]	4.89844e-05
TH	[NCBI]	3.8685e-05
SCN5A	[NCBI]	3.29352e-05
VIP	[NCBI]	2.72702e-05
BMP4	[NCBI]	2.37496e-05
NPPA	[NCBI]	2.21367e-05
CEACAM5	[NCBI]	1.91816e-05
GJA1	[NCBI]	1.61112e-05
COMT	[NCBI]	1.45626e-05
RA	[NCBI]	1.12536e-05
PCNA	[NCBI]	3.46126e-06