MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
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