|
OMIM |
Link |
Information
gain |
01 |
|
|
nevi flammei, familial multiple
|
[NCBI]
|
0.0043503
|
|
|
|
klippel-trenaunay-weber syndrome
|
[NCBI]
|
0.000990409
|
|
|
|
telangiectasia, hereditary benign
|
[NCBI]
|
0.000844965
|
|
|
|
hemangioma, capillary infantile
|
[NCBI]
|
0.000773718
|
|
|
|
sturge-weber syndrome
|
[NCBI]
|
0.000367457
|
|
|
|
capillary malformation-arteriovenous malformation
|
[NCBI]
|
0.000311544
|
|
|
|
parkes weber syndrome
|
[NCBI]
|
0.000154415
|
|
|
|
velofacioskeletal syndrome
|
[NCBI]
|
0.000131943
|
|
|
|
RASA1
|
[NCBI]
|
0.000129469
|
|
|
|
CCM2
|
[NCBI]
|
0.00011386
|
|
|
|
CCM3
|
[NCBI]
|
0.000107884
|
|
|
|
VMCM
|
[NCBI]
|
0.000107884
|
|
|
|
GVM
|
[NCBI]
|
9.37927e-05
|
|
|
|
CMTC
|
[NCBI]
|
7.63662e-05
|
|
|
|
KRIT1
|
[NCBI]
|
7.25879e-05
|
|
|
|
HHT
|
[NCBI]
|
6.50911e-05
|
|
