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MeSH keywords -> Related genes, diseases (OMIM)


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01 Telangiectasia, Hereditary Hemorrhagic [NCBI]

Gene


 Gene Link Information
Gain		 01
ENG [NCBI] 0.00132611
ACVRL1 [NCBI] 0.000952725
BMPR2 [NCBI] 0.000105944
TGFBR1 [NCBI] 4.38016e-05
SMAD4 [NCBI] 3.30201e-05
BMPR1A [NCBI] 1.52664e-05
GDF2 [NCBI] 1.0118e-05
VEGFA [NCBI] 8.88411e-06
ACVR2A [NCBI] 8.23288e-06
ALCAM [NCBI] 7.12708e-06
ACVR1 [NCBI] 6.57659e-06
TGFB3 [NCBI] 6.46301e-06
TGFB1 [NCBI] 6.1477e-06
KRIT1 [NCBI] 5.44936e-06
ABCC6 [NCBI] 5.02767e-06
ALK [NCBI] 2.95091e-06
PMP22 [NCBI] 2.80786e-06
F8 [NCBI] 2.79655e-06
CDH1 [NCBI] 2.702e-06
CCL2 [NCBI] 1.92805e-06
NOS3 [NCBI] 1.04514e-06
PTEN [NCBI] 9.82754e-07
MLH1 [NCBI] 9.29961e-07
VWF [NCBI] 5.26017e-07
TNF [NCBI] 1.91233e-07
EGF [NCBI] 3.78799e-08



OMIM


 OMIM Link Information
gain		 01
HHT [NCBI] 0.00888112
ORW3 [NCBI] 0.00425713
ORW2 [NCBI] 0.0024448
ENG [NCBI] 0.00242721
ACVRL1 [NCBI] 0.00156322
CMTC [NCBI] 0.000292846
JPHT [NCBI] 0.000157072
VMCM [NCBI] 0.000151113
pulmonary arteriovenous fistulas [NCBI] 0.000109376
PPH1 [NCBI] 0.000102599
SMAD4 [NCBI] 8.63825e-05
JPS [NCBI] 8.12152e-05
musical perfect pitch [NCBI] 6.29518e-05
epstein syndrome [NCBI] 5.52436e-05
von willebrand disease [NCBI] 5.42749e-05
ehlers-danlos syndrome, type ii [NCBI] 5.37868e-05
COL5A1 [NCBI] 4.27023e-05
KRIT1 [NCBI] 4.12342e-05
mucopolysaccharidosis type iva [NCBI] 2.8593e-05
CCM [NCBI] 2.85642e-05
TGFB1 [NCBI] 2.84094e-05
ALS1 [NCBI] 2.33648e-05
VEGF [NCBI] 1.90504e-05
TNF [NCBI] 7.8093e-06
EGF [NCBI] 1.88376e-06



Database Center for Life Science