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MeSH keywords -> Related genes, diseases (OMIM)


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01 Marfan Syndrome [NCBI]

Gene


 Gene Link Information
Gain		 01
FBN1 [NCBI] 0.00142882
MYP3 [NCBI] 0.000332278
MYP2 [NCBI] 0.000306322
TGFBR1 [NCBI] 9.73895e-05
TGFBR2 [NCBI] 9.49086e-05
FBN2 [NCBI] 9.04511e-05
GER [NCBI] 7.73885e-05
EGF [NCBI] 2.91722e-05
LAMB1 [NCBI] 1.74165e-05
DCN [NCBI] 1.59031e-05
MFAP1 [NCBI] 1.48846e-05
FBN3 [NCBI] 1.16061e-05
ZDHHC9 [NCBI] 1.16061e-05
LTBP3 [NCBI] 1.10229e-05
FBLN2 [NCBI] 1.05893e-05
MMACHC [NCBI] 9.13326e-06
ELA1 [NCBI] 9.13326e-06
LTBP2 [NCBI] 8.83427e-06
LTBP1 [NCBI] 7.42335e-06
SDC4 [NCBI] 7.19899e-06
TGFB1 [NCBI] 6.4818e-06
ELN [NCBI] 5.7419e-06
KISS1 [NCBI] 5.42048e-06
EDA [NCBI] 5.26369e-06
FGF4 [NCBI] 5.21455e-06
COL3A1 [NCBI] 5.18259e-06
BMI1 [NCBI] 5.06057e-06
VCAN [NCBI] 4.57963e-06
TGFB2 [NCBI] 4.14048e-06
IBSP [NCBI] 4.14048e-06
PAX3 [NCBI] 3.86489e-06
SMAD2 [NCBI] 3.77606e-06
CD44 [NCBI] 3.71738e-06
NOTCH1 [NCBI] 3.57669e-06
PTPN11 [NCBI] 3.25092e-06
MMP2 [NCBI] 2.83217e-06
AGT [NCBI] 2.44807e-06
ACE [NCBI] 1.51031e-06
MTHFR [NCBI] 1.22207e-06
VWF [NCBI] 6.026e-07



OMIM


 OMIM Link Information
gain		 01
MFS [NCBI] 0.0229559
FBN1 [NCBI] 0.0067501
VDEGS [NCBI] 0.00368744
contractural arachnodactyly, congenital [NCBI] 0.00205046
aortic aneurysm, familial thoracic 1 [NCBI] 0.00126994
marden-walker syndrome [NCBI] 0.00103444
joint laxity, familial [NCBI] 0.000785962
RA [NCBI] 0.000761993
shprintzen-goldberg craniosynostosis syndrome [NCBI] 0.000746811
CVD1 [NCBI] 0.000650784
MYP3 [NCBI] 0.000650784
MFS2 [NCBI] 0.000568974
SLE [NCBI] 0.000553833
LDS [NCBI] 0.000501024
MYP2 [NCBI] 0.000429633
marfanoid hypermobility syndrome [NCBI] 0.000417495
LAMB1 [NCBI] 0.000378039
lujan-fryns syndrome [NCBI] 0.000375633
ectopia lentis, isolated [NCBI] 0.000375633
GPS [NCBI] 0.000321809
MVP [NCBI] 0.000307355
EEC1 [NCBI] 0.000298481
mass syndrome [NCBI] 0.000276597
TGFBR2 [NCBI] 0.00026716
furlong syndrome: fs [NCBI] 0.000240189
diverticulosis of bowel, hernia, and retinal detachment [NCBI] 0.000184344
TGFBR1 [NCBI] 0.000146121
MFAP1 [NCBI] 0.000135273
aortic valve disease [NCBI] 0.000134805
TGFB1 [NCBI] 0.000129593
DCN [NCBI] 0.000120797
HMS [NCBI] 0.000111748
pneumothorax, primary spontaneous [NCBI] 9.72472e-05
microspherophakia with hernia [NCBI] 9.21455e-05
aortic aneurysm, familial thoracic 5 [NCBI] 9.21455e-05
marfanoid habitus with situs inversus [NCBI] 9.21455e-05
achard syndrome [NCBI] 9.21455e-05
marfanoid mental retardation syndrome, autosomal [NCBI] 9.21455e-05
marfanoid habitus with microcephaly and glomerulonephritis [NCBI] 9.21455e-05
sella turcica, bridged [NCBI] 9.21455e-05
COL1A2 [NCBI] 7.70386e-05
aortic aneurysm, familial thoracic 3 [NCBI] 6.97279e-05
homocystinuria [NCBI] 6.78745e-05
ZDHHC9 [NCBI] 6.76055e-05
FBN3 [NCBI] 6.76055e-05
MEN2B [NCBI] 6.37407e-05
IS1 [NCBI] 6.34945e-05
retinopathy, pigmentary, and mental retardation [NCBI] 6.13008e-05
ehlers-danlos syndrome, type i [NCBI] 5.93071e-05
weill-marchesani syndrome, autosomal dominant [NCBI] 5.58476e-05
internal carotid artery, spontaneous dissection of [NCBI] 5.58476e-05
pierre robin syndrome [NCBI] 5.58476e-05
ectopia lentis [NCBI] 5.58476e-05
craniosynostosis with ectopia lentis [NCBI] 5.58476e-05
FBLN2 [NCBI] 5.38358e-05
P4HA3 [NCBI] 5.38358e-05
ELA1 [NCBI] 5.38358e-05
ELN [NCBI] 4.8742e-05
SCA5 [NCBI] 4.59385e-05
phace association [NCBI] 4.36698e-05
PMS1 [NCBI] 4.27779e-05
MED12 [NCBI] 4.27779e-05
weill-marchesani syndrome, autosomal recessive [NCBI] 3.99435e-05
ehlers-danlos syndrome, type vii, autosomal dominant [NCBI] 3.69542e-05
SVAS [NCBI] 3.59761e-05
LADD [NCBI] 3.56569e-05
osteogenesis imperfecta, type i [NCBI] 3.53048e-05
GNB3 [NCBI] 3.44046e-05
FMD [NCBI] 3.04759e-05
tay-sachs disease, ab variant [NCBI] 2.94015e-05
GLB1 [NCBI] 2.31221e-05
ABS [NCBI] 2.26709e-05
EGF [NCBI] 2.25183e-05
ornithine aminotransferase deficiency [NCBI] 2.17943e-05
CEACAM5 [NCBI] 2.04768e-05
ehlers-danlos syndrome, type iv, autosomal dominant [NCBI] 1.88503e-05
exostoses, multiple, type i [NCBI] 1.84897e-05
cardiofaciocutaneous syndrome [NCBI] 1.81395e-05
COH1 [NCBI] 1.74684e-05
costello syndrome [NCBI] 1.43434e-05
APC [NCBI] 9.78123e-06
CCD [NCBI] 8.64337e-06
MEN2A [NCBI] 8.11423e-06
NS1 [NCBI] 7.04066e-06
ACH [NCBI] 4.87618e-06
NF1 [NCBI] 3.74429e-06
TS [NCBI] 3.5244e-06
KSS [NCBI] 2.82432e-06
DMD [NCBI] 1.47066e-06
polycystic kidneys [NCBI] 6.42474e-07
PXE [NCBI] 4.5044e-07
HD [NCBI] 4.43067e-07
dystrophia myotonica 1 [NCBI] 3.77293e-07
VRNI [NCBI] 3.15914e-07



Database Center for Life Science