MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Heart Valve Diseases
[NCBI]
Gene
Gene
Link
Information
Gain
01
LECT1
[NCBI]
2.18016e-05
CD68
[NCBI]
1.90762e-05
TGFB1
[NCBI]
1.65138e-05
COL1A2
[NCBI]
1.63913e-05
VWF
[NCBI]
1.61052e-05
NPPA
[NCBI]
1.55394e-05
MGP
[NCBI]
1.44561e-05
ACE
[NCBI]
1.42119e-05
MMP1
[NCBI]
1.2949e-05
NOTCH1
[NCBI]
1.26025e-05
TNMD
[NCBI]
1.1538e-05
LTBP1
[NCBI]
9.00076e-06
FLNA
[NCBI]
8.16216e-06
KCNJ2
[NCBI]
8.09008e-06
LRP5
[NCBI]
7.89049e-06
CD59
[NCBI]
7.85938e-06
CXCL16
[NCBI]
7.85938e-06
TAGLN
[NCBI]
7.79882e-06
TNF
[NCBI]
7.62348e-06
TH
[NCBI]
7.56065e-06
KCNE1
[NCBI]
7.33324e-06
IL1R1
[NCBI]
7.06194e-06
FGF4
[NCBI]
6.77844e-06
COL3A1
[NCBI]
6.74612e-06
TIMP2
[NCBI]
6.74612e-06
SFN
[NCBI]
6.56418e-06
CS
[NCBI]
6.53567e-06
ITPR1
[NCBI]
6.46644e-06
NPPB
[NCBI]
6.26225e-06
DBH
[NCBI]
6.25028e-06
TIMP1
[NCBI]
6.13498e-06
JAG1
[NCBI]
5.71345e-06
BMP4
[NCBI]
5.46432e-06
VEGFA
[NCBI]
5.37313e-06
MMP13
[NCBI]
4.91093e-06
PTPN11
[NCBI]
4.77265e-06
TGFBR1
[NCBI]
4.60474e-06
GZMB
[NCBI]
4.46468e-06
MMP2
[NCBI]
4.33575e-06
MMP9
[NCBI]
3.96215e-06
AGT
[NCBI]
3.92976e-06
PTH
[NCBI]
3.90154e-06
IL10
[NCBI]
3.09947e-06
CALCA
[NCBI]
3.01654e-06
TRH
[NCBI]
2.96578e-06
IL6
[NCBI]
2.59077e-06
AVP
[NCBI]
2.57518e-06
IL1RN
[NCBI]
2.3018e-06
MPO
[NCBI]
1.70013e-06
CDKN1A
[NCBI]
1.15943e-06
PTGS2
[NCBI]
9.7876e-07
OMIM
OMIM
Link
Information
gain
01
MVP
[NCBI]
0.00434391
CVD1
[NCBI]
0.0017432
singleton-merten syndrome
[NCBI]
0.000862873
aortic valve disease
[NCBI]
0.000690898
geleophysic dysplasia
[NCBI]
0.000570957
SLE
[NCBI]
0.000497154
gaucher disease, type iiic
[NCBI]
0.00035809
ehlers-danlos syndrome, autosomal recessive, cardiac valvular form
[NCBI]
0.000192656
AVSD
[NCBI]
0.000187728
calcific aortic disease with immunologic abnormalities, familial
[NCBI]
0.000169094
GBA
[NCBI]
0.000126403
disproportionate short stature with ptosis and valvular heart lesions
[NCBI]
0.000111707
LECT1
[NCBI]
8.48492e-05
ehlers-danlos-like syndrome due to tenascin-x deficiency
[NCBI]
8.07854e-05
COL1A2
[NCBI]
7.74782e-05
MFS
[NCBI]
7.58431e-05
marfanoid hypermobility syndrome
[NCBI]
6.79662e-05
ABCG8
[NCBI]
5.99851e-05
NPPA
[NCBI]
5.81863e-05
LAMB1
[NCBI]
5.63228e-05
ehlers-danlos syndrome, type ii
[NCBI]
5.60904e-05
CMH
[NCBI]
5.34151e-05
sitosterolemia
[NCBI]
5.1315e-05
kawasaki disease
[NCBI]
5.1315e-05
HGD
[NCBI]
4.90631e-05
NOTCH1
[NCBI]
4.49227e-05
alkaptonuria
[NCBI]
4.1653e-05
HRPT1
[NCBI]
4.05862e-05
AGT
[NCBI]
4.00649e-05
FLNA
[NCBI]
3.9218e-05
ehlers-danlos syndrome, type i
[NCBI]
3.73515e-05
sandhoff disease
[NCBI]
3.50439e-05
GUSB
[NCBI]
3.01875e-05
TH
[NCBI]
2.4085e-05
NS1
[NCBI]
2.28465e-05
hypercholesterolemia, autosomal dominant
[NCBI]
2.22604e-05
LDLR
[NCBI]
2.13528e-05
RA
[NCBI]
1.38738e-05
SPP1
[NCBI]
1.22613e-05
PXE
[NCBI]
1.11384e-05
PD
[NCBI]
8.85959e-06
TNF
[NCBI]
7.70605e-06
PTH
[NCBI]
7.02378e-06
polycystic kidneys
[NCBI]
5.34985e-06
AVP
[NCBI]
4.05919e-06
MPO
[NCBI]
2.50195e-06
MG
[NCBI]
2.0614e-06
VEGF
[NCBI]
6.83686e-07
Database Center for Life Science