Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Aortic Valve Insufficiency	[NCBI]

Gene	Link	Information Gain
FBN1	[NCBI]	2.10686e-05
NPPB	[NCBI]	2.05719e-05
ACE	[NCBI]	1.36466e-05
MASP2	[NCBI]	1.12461e-05
CTSA	[NCBI]	1.04423e-05
BMP4	[NCBI]	8.20727e-06
MBL2	[NCBI]	7.90975e-06
NOTCH1	[NCBI]	7.84741e-06
PTPN11	[NCBI]	7.50478e-06
HLA-DQB1	[NCBI]	6.13715e-06
HLA-DRB1	[NCBI]	5.51401e-06

OMIM	Link	Information gain
aortic valve disease	[NCBI]	0.00181649
CVD1	[NCBI]	0.00123814
calcific aortic disease with immunologic abnormalities, familial	[NCBI]	0.000301817
MFS	[NCBI]	0.000199831
CMH	[NCBI]	0.00017735
marfanoid habitus with situs inversus	[NCBI]	0.000118506
sella turcica, bridged	[NCBI]	0.000118506
AVSD	[NCBI]	8.45636e-05
ectopia lentis, isolated	[NCBI]	6.97197e-05
PTPN11	[NCBI]	6.27854e-05
ATS	[NCBI]	6.14849e-05
neuraminidase deficiency with beta-galactosidase deficiency	[NCBI]	5.60164e-05
alkaptonuria	[NCBI]	4.82931e-05
COL1A1	[NCBI]	4.75757e-05
FBN1	[NCBI]	4.67174e-05
EFE	[NCBI]	4.62069e-05
hurler syndrome	[NCBI]	3.52008e-05
temporal arteritis	[NCBI]	3.31811e-05
NPPA	[NCBI]	2.61937e-05
SLE	[NCBI]	2.50428e-05
RA	[NCBI]	2.36706e-05
EGFR	[NCBI]	1.34837e-05
polycystic kidneys	[NCBI]	9.97911e-06