MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Aortic Valve Stenosis
[NCBI]
Gene
Gene
Link
Information
Gain
01
FRA12A
[NCBI]
0.000438875
HNRPA1L-2
[NCBI]
0.000438875
ELN
[NCBI]
8.57544e-05
TGFB1
[NCBI]
2.70347e-05
C3
[NCBI]
1.66729e-05
BMP2
[NCBI]
1.65082e-05
TNFRSF11A
[NCBI]
1.5672e-05
TNFSF11
[NCBI]
1.4963e-05
ACE
[NCBI]
1.32457e-05
APOE
[NCBI]
1.31963e-05
JARID2
[NCBI]
1.22794e-05
OGN
[NCBI]
1.03886e-05
PCBP1
[NCBI]
1.00893e-05
VWF
[NCBI]
9.67606e-06
NPPC
[NCBI]
9.61295e-06
HCN4
[NCBI]
9.32644e-06
HNRNPK
[NCBI]
9.08109e-06
SFRS2
[NCBI]
9.00655e-06
KLF2
[NCBI]
8.80063e-06
TNFRSF11B
[NCBI]
8.50909e-06
CDK9
[NCBI]
8.50451e-06
C5
[NCBI]
8.34871e-06
RHEB
[NCBI]
8.25221e-06
C5AR1
[NCBI]
8.20594e-06
C4B
[NCBI]
8.20594e-06
AHSG
[NCBI]
7.91302e-06
CCL26
[NCBI]
7.76577e-06
PLA2G7
[NCBI]
7.69666e-06
TXNIP
[NCBI]
7.63025e-06
C3AR1
[NCBI]
7.47474e-06
AOC3
[NCBI]
7.35981e-06
AGTR2
[NCBI]
7.35981e-06
ADAR
[NCBI]
7.0788e-06
IL6
[NCBI]
6.81501e-06
AVP
[NCBI]
6.78259e-06
COL1A2
[NCBI]
6.66328e-06
TIMP2
[NCBI]
6.42324e-06
COL3A1
[NCBI]
6.42324e-06
FBN1
[NCBI]
6.18515e-06
RUNX2
[NCBI]
6.13053e-06
NPPB
[NCBI]
5.94023e-06
TIMP1
[NCBI]
5.81322e-06
MGP
[NCBI]
5.70557e-06
CXCL9
[NCBI]
5.61427e-06
APOA1
[NCBI]
5.37555e-06
IBSP
[NCBI]
5.36702e-06
COL1A1
[NCBI]
5.15933e-06
BMP4
[NCBI]
5.14438e-06
SELPLG
[NCBI]
5.0931e-06
ADM
[NCBI]
5.05038e-06
FGF23
[NCBI]
4.8211e-06
NOTCH1
[NCBI]
4.79081e-06
BMP7
[NCBI]
4.77885e-06
CTSG
[NCBI]
4.68056e-06
ERBB4
[NCBI]
4.60383e-06
SLC2A4
[NCBI]
4.59848e-06
PTPN11
[NCBI]
4.45553e-06
EGR1
[NCBI]
4.35143e-06
TGFBR1
[NCBI]
4.28851e-06
PLN
[NCBI]
4.08975e-06
CCR5
[NCBI]
4.07424e-06
SLC2A1
[NCBI]
4.01741e-06
TLR2
[NCBI]
3.62396e-06
AGT
[NCBI]
3.61817e-06
CTGF
[NCBI]
3.49593e-06
APOB
[NCBI]
3.3926e-06
CST3
[NCBI]
3.04549e-06
CXCL12
[NCBI]
3.02378e-06
IL10
[NCBI]
2.7971e-06
VDR
[NCBI]
2.7154e-06
TLR4
[NCBI]
2.5547e-06
MTHFR
[NCBI]
2.27721e-06
EPO
[NCBI]
1.45608e-06
PCNA
[NCBI]
1.23897e-06
CDKN1A
[NCBI]
9.19038e-07
TNF
[NCBI]
1.03135e-07
OMIM
OMIM
Link
Information
gain
01
SVAS
[NCBI]
0.00395889
aortic aneurysm, familial thoracic 1
[NCBI]
0.00335645
WBS
[NCBI]
0.00219108
aortic valve disease
[NCBI]
0.00142678
ELN
[NCBI]
0.00064613
calcific aortic disease with immunologic abnormalities, familial
[NCBI]
0.000528872
RA
[NCBI]
0.00030167
EFE
[NCBI]
0.000154697
hypercalcemia, idiopathic, of infancy
[NCBI]
0.000143409
CMH
[NCBI]
0.00012648
ARH
[NCBI]
0.000120965
SLE
[NCBI]
0.000114321
scheie syndrome
[NCBI]
0.000109773
AVSD
[NCBI]
0.000108505
pfeiffer-palm-teller syndrome
[NCBI]
0.000105527
alkaptonuria
[NCBI]
9.38464e-05
mucopolysaccharidosis type vi
[NCBI]
8.8637e-05
subaortic stenosis, membranous
[NCBI]
8.30787e-05
OBSCN
[NCBI]
8.29498e-05
mental retardation, fra12a type
[NCBI]
6.18244e-05
CDK9
[NCBI]
6.05968e-05
ectopia lentis, isolated
[NCBI]
5.68344e-05
NPPA
[NCBI]
5.26549e-05
fibromuscular dysplasia of arteries
[NCBI]
4.63073e-05
PTPN11
[NCBI]
4.25603e-05
AFD1
[NCBI]
3.93755e-05
dyschromatosis symmetrica hereditaria 1
[NCBI]
3.62424e-05
CALCRL
[NCBI]
3.51634e-05
SPP1
[NCBI]
3.38414e-05
TNFRSF11B
[NCBI]
3.37813e-05
BSG
[NCBI]
3.28644e-05
MFS
[NCBI]
2.80653e-05
FBN1
[NCBI]
2.66712e-05
von willebrand disease
[NCBI]
2.54189e-05
bullous erythroderma ichthyosiformis congenita of brocq
[NCBI]
2.35425e-05
ADM
[NCBI]
2.30201e-05
GJA1
[NCBI]
2.24921e-05
osteogenesis imperfecta, type i
[NCBI]
1.94165e-05
AVP
[NCBI]
1.56254e-05
CTGF
[NCBI]
1.55014e-05
FRDA
[NCBI]
1.49815e-05
APOE
[NCBI]
1.39059e-05
VEGF
[NCBI]
3.18362e-06
EPO
[NCBI]
1.5409e-06
PCNA
[NCBI]
9.0011e-07
EGFR
[NCBI]
2.08268e-07
thrombocytopenic purpura, autoimmune
[NCBI]
1.49013e-07
FMF
[NCBI]
3.06713e-08
Database Center for Life Science