|
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
|
|
