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MeSH keywords -> Related genes, diseases (OMIM)


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01 Arteriovenous Malformations [NCBI]


Gene


Gene Link Information
Gain
01
KTWS [NCBI] 0.000332969
ENG [NCBI] 0.000197191
ACVRL1 [NCBI] 0.000185162
RASA1 [NCBI] 3.49667e-05
PTEN [NCBI] 1.43867e-05
VTNR [NCBI] 1.32065e-05
SMAD4 [NCBI] 1.18166e-05
EFNB2 [NCBI] 1.01668e-05
DLL4 [NCBI] 1.00071e-05
EPHB2 [NCBI] 9.60165e-06
TAGLN [NCBI] 8.3987e-06
FOXC2 [NCBI] 8.099e-06
WT1 [NCBI] 6.54144e-06
APOE [NCBI] 6.07337e-06
SLC2A1 [NCBI] 4.91843e-06
HMOX1 [NCBI] 4.88475e-06
NPY [NCBI] 2.84622e-06
TNF [NCBI] 2.79133e-06
HIF1A [NCBI] 2.78664e-06
HGF [NCBI] 2.76251e-06
AR [NCBI] 2.32262e-06
PCNA [NCBI] 2.00613e-06




OMIM


OMIM Link Information
gain
01
angioma, hereditary neurocutaneous [NCBI] 0.00254276
klippel-trenaunay-weber syndrome [NCBI] 0.00184884
HHT [NCBI] 0.000814299
hemangioma, capillary infantile [NCBI] 0.000626524
nevi flammei, familial multiple [NCBI] 0.000600386
thrombocytopenia-absent radius syndrome [NCBI] 0.000361716
AOS [NCBI] 0.000319021
proteus syndrome [NCBI] 0.000298436
ORW2 [NCBI] 0.000249379
ENG [NCBI] 0.000235376
CD [NCBI] 0.000165728
pulmonary arteriovenous fistulas [NCBI] 0.00012988
lymphedema and cerebral arteriovenous anomaly [NCBI] 0.00012988
parkes weber syndrome [NCBI] 0.00012988
CCM [NCBI] 0.000119576
BRRS [NCBI] 0.000118468
ACVRL1 [NCBI] 0.000110727
capillary malformation-arteriovenous malformation [NCBI] 0.000107412
vascular malformation, primary intraosseous [NCBI] 0.000107412
pulmonary hypertension, familial persistent, of the newborn [NCBI] 8.93415e-05
JPHT [NCBI] 8.60827e-05
arteriovenous malformations of the brain [NCBI] 8.60827e-05
VMCM [NCBI] 8.33736e-05
lymphedema, hereditary, ii [NCBI] 7.72292e-05
PTEN [NCBI] 7.66507e-05
PDV [NCBI] 7.56107e-05
GVM [NCBI] 6.93203e-05
KLF2 [NCBI] 6.28306e-05
DLL4 [NCBI] 5.97434e-05
EPHX1 [NCBI] 4.68441e-05
HMI [NCBI] 4.18593e-05
WT1 [NCBI] 3.99396e-05
RASA1 [NCBI] 3.58681e-05
von willebrand disease [NCBI] 3.20239e-05
MFS [NCBI] 2.53937e-05
VEGF [NCBI] 1.51569e-05
HGF [NCBI] 8.67121e-06
NPY [NCBI] 8.49744e-06
AR [NCBI] 7.379e-06
thrombocytopenic purpura, autoimmune [NCBI] 4.99775e-06
PCNA [NCBI] 4.55026e-06




Database Center for Life Science