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MeSH keywords -> Related genes, diseases (OMIM)


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01 Mitral Valve Prolapse [NCBI]

Gene


 Gene Link Information
Gain		 01
MMVP1 [NCBI] 0.000438875
MMVP2 [NCBI] 0.000438875
FBN1 [NCBI] 4.13144e-05
AGT [NCBI] 2.14793e-05
TSHR [NCBI] 1.84074e-05
PF4 [NCBI] 1.43443e-05
CHAT [NCBI] 1.24697e-05
HSPG2 [NCBI] 1.07349e-05
ACE [NCBI] 1.07212e-05
NPY [NCBI] 9.42055e-06
TNXB [NCBI] 9.34802e-06
GFAP [NCBI] 8.29982e-06
COL3A1 [NCBI] 8.06967e-06
PLAU [NCBI] 7.3366e-06
MMP3 [NCBI] 6.86517e-06
MMP1 [NCBI] 6.59505e-06
AGTR1 [NCBI] 6.16285e-06
PTPN11 [NCBI] 6.0813e-06
POMC [NCBI] 6.05661e-06
IL4 [NCBI] 5.60019e-06
IL1B [NCBI] 4.70905e-06
IL10 [NCBI] 4.37001e-06
BDNF [NCBI] 3.97102e-06
IL1RN [NCBI] 3.53288e-06
HIF1A [NCBI] 3.46844e-06
TGFB1 [NCBI] 3.08408e-06
VWF [NCBI] 2.98536e-06



OMIM


 OMIM Link Information
gain		 01
MVP [NCBI] 0.0138176
MMVP2 [NCBI] 0.000945056
MMVP3 [NCBI] 0.000945056
borrone dermatocardioskeletal syndrome [NCBI] 0.000945056
CVD1 [NCBI] 0.000592537
camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormal palmar creases [NCBI] 0.000495958
PAND1 [NCBI] 0.000454472
MFS [NCBI] 0.000247496
FBN1 [NCBI] 0.000192112
ectopia lentis, isolated [NCBI] 0.000183236
disproportionate short stature with ptosis and valvular heart lesions [NCBI] 0.000127818
hypertaurinuric cardiomyopathy [NCBI] 0.000127818
hydrocephalus, tall stature, joint laxity, and kyphoscoliosis [NCBI] 0.000127818
lymphedema-hypoparathyroidism syndrome [NCBI] 0.000127818
COH1 [NCBI] 0.000125241
mass syndrome [NCBI] 9.68753e-05
TSHR [NCBI] 9.32168e-05
orthostatic intolerance [NCBI] 8.40249e-05
fragile x mental retardation syndrome [NCBI] 8.17863e-05
NPPA [NCBI] 7.27882e-05
dystrophia myotonica 1 [NCBI] 7.06709e-05
FMD [NCBI] 6.53139e-05
PF4 [NCBI] 5.7744e-05
ehlers-danlos syndrome, type i [NCBI] 5.30777e-05
STL1 [NCBI] 5.26571e-05
TRPS2 [NCBI] 5.10787e-05
RA [NCBI] 4.85516e-05
CHAT [NCBI] 4.63911e-05
aortic valve disease [NCBI] 4.59951e-05
HOS [NCBI] 4.54622e-05
contractural arachnodactyly, congenital [NCBI] 4.40399e-05
SVAS [NCBI] 4.05667e-05
TGFB1 [NCBI] 4.02585e-05
osteogenesis imperfecta, type i [NCBI] 4.01904e-05
fabry disease [NCBI] 3.49132e-05
von willebrand disease [NCBI] 3.20239e-05
CMH [NCBI] 3.11294e-05
KSS [NCBI] 3.10287e-05
NPY [NCBI] 2.94333e-05
DMD [NCBI] 2.8052e-05
WBS [NCBI] 2.70323e-05
ACE [NCBI] 2.42253e-05
GFAP [NCBI] 2.35292e-05
NF1 [NCBI] 2.26257e-05
polycystic kidneys [NCBI] 1.74727e-05
MDD [NCBI] 1.25289e-05
SLE [NCBI] 1.18332e-05
BDNF [NCBI] 1.11154e-05



Database Center for Life Science