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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