Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Aortic Aneurysm	[NCBI]

Gene	Link	Information Gain
AAT1	[NCBI]	0.000499621
FBN1	[NCBI]	4.75569e-05
TGFBR2	[NCBI]	3.83725e-05
COL3A1	[NCBI]	3.73909e-05
MMP9	[NCBI]	2.60114e-05
TGFBR1	[NCBI]	1.99623e-05
ZFAND2B	[NCBI]	1.66232e-05
TMBIM1	[NCBI]	1.33444e-05
APOE	[NCBI]	9.84904e-06
LAMB1	[NCBI]	9.21792e-06
CMA1	[NCBI]	8.93157e-06
CALCA	[NCBI]	8.63285e-06
NOX1	[NCBI]	8.55451e-06
ACE	[NCBI]	8.39661e-06
TNXB	[NCBI]	8.17663e-06
TNC	[NCBI]	7.86744e-06
XDH	[NCBI]	7.75793e-06
CTSB	[NCBI]	7.73161e-06
LAMA1	[NCBI]	7.58174e-06
CD68	[NCBI]	7.47823e-06
ELN	[NCBI]	7.4662e-06
MB	[NCBI]	6.54182e-06
CNN1	[NCBI]	6.32344e-06
PLAU	[NCBI]	6.17121e-06
JAG1	[NCBI]	5.86767e-06
TGFB2	[NCBI]	5.84184e-06
CD44	[NCBI]	5.40783e-06
HSPB1	[NCBI]	5.17464e-06
OSM	[NCBI]	5.1519e-06
CTSG	[NCBI]	5.1519e-06
SDC1	[NCBI]	4.97028e-06
PRKCB	[NCBI]	4.77497e-06
TFPI	[NCBI]	4.62488e-06
GZMB	[NCBI]	4.61671e-06
F8	[NCBI]	4.57247e-06
PKD1	[NCBI]	4.43556e-06
CTSL1	[NCBI]	4.27264e-06
CETP	[NCBI]	3.47708e-06
MTHFR	[NCBI]	2.71318e-06
TGFB1	[NCBI]	2.0198e-06
GFAP	[NCBI]	1.92941e-06
FASLG	[NCBI]	1.88487e-06
VEGFA	[NCBI]	1.75818e-06
PTH	[NCBI]	1.09706e-06

OMIM	Link	Information gain
aortic aneurysm, familial thoracic 1	[NCBI]	0.00750153
MFS	[NCBI]	0.00145186
aortic aneurysm, abdominal	[NCBI]	0.0010809
CVD1	[NCBI]	0.000744944
aortic valve disease	[NCBI]	0.000721878
temporal arteritis	[NCBI]	0.000435042
behcet syndrome	[NCBI]	0.000334214
COL3A1	[NCBI]	0.000207785
aortic aneurysm, giant congenital	[NCBI]	0.000198565
FBN1	[NCBI]	0.00017599
LDS	[NCBI]	0.00013918
TGFBR2	[NCBI]	0.000102256
heterotopia, periventricular, ehlers-danlos variant	[NCBI]	7.82229e-05
furlong syndrome: fs	[NCBI]	7.82229e-05
aortic aneurysm, familial thoracic 4	[NCBI]	7.82229e-05
menkes disease	[NCBI]	7.62897e-05
TMBIM1	[NCBI]	7.2176e-05
phace association	[NCBI]	6.58794e-05
ectopia lentis, isolated	[NCBI]	6.58794e-05
MFS2	[NCBI]	6.38614e-05
shprintzen-goldberg craniosynostosis syndrome	[NCBI]	6.04601e-05
fibromuscular dysplasia of arteries	[NCBI]	5.52795e-05
cutis laxa, autosomal dominant	[NCBI]	5.52795e-05
TGFBR1	[NCBI]	5.476e-05
ORW2	[NCBI]	4.8988e-05
MYH11	[NCBI]	4.31157e-05
contractural arachnodactyly, congenital	[NCBI]	4.03164e-05
ehlers-danlos syndrome, type iv, autosomal dominant	[NCBI]	3.9775e-05
APOE	[NCBI]	3.91793e-05
MMP9	[NCBI]	3.77166e-05
ELN	[NCBI]	3.5498e-05
TNC	[NCBI]	3.10631e-05
ALGS1	[NCBI]	3.06235e-05
ABP1	[NCBI]	2.91704e-05
HHT	[NCBI]	2.64663e-05
OSM	[NCBI]	2.55688e-05
TS	[NCBI]	2.33381e-05
TFPI	[NCBI]	1.71284e-05
XDH	[NCBI]	1.69456e-05
SPP1	[NCBI]	1.32406e-05
SLE	[NCBI]	1.11427e-05
GFAP	[NCBI]	3.38411e-06
PTH	[NCBI]	6.24883e-07
VEGF	[NCBI]	5.89348e-07