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MeSH keywords -> Related genes, diseases (OMIM)


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01 Aortic Aneurysm [NCBI]


Gene


Gene Link Information
Gain
01
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


OMIM Link Information
gain
01
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




Database Center for Life Science