|
OMIM |
Link |
Information gain |
01 |
|
klippel-trenaunay-weber syndrome
|
[NCBI]
|
0.00116638
|
|
|
fibromuscular dysplasia of arteries
|
[NCBI]
|
0.000510601
|
|
|
GACI
|
[NCBI]
|
0.000268367
|
|
|
NF1
|
[NCBI]
|
0.000253266
|
|
|
SLE
|
[NCBI]
|
0.000221883
|
|
|
NPPA
|
[NCBI]
|
0.000182443
|
|
|
arterial occlusive disease, progressive, with hypertension, heart defects, bone fragility, and brachysyndactyly
|
[NCBI]
|
0.000179592
|
|
|
brain small vessel disease with hemorrhage
|
[NCBI]
|
0.000179592
|
|
|
autoimmune disease
|
[NCBI]
|
0.000142325
|
|
|
renal cell carcinoma, papillary
|
[NCBI]
|
0.000142325
|
|
|
NPY
|
[NCBI]
|
0.000129204
|
|
|
temporal arteritis
|
[NCBI]
|
0.000119042
|
|
|
AVP
|
[NCBI]
|
7.4274e-05
|
|
|
ADM
|
[NCBI]
|
5.26225e-05
|
|
|
FMF
|
[NCBI]
|
4.37131e-05
|
|
|
TS
|
[NCBI]
|
3.44416e-05
|
|
|
RA
|
[NCBI]
|
3.28056e-05
|
|
|
COL4A1
|
[NCBI]
|
2.74177e-05
|
|
|
AGTR1
|
[NCBI]
|
2.43554e-05
|
|
|
NOS3
|
[NCBI]
|
2.17472e-05
|
|
|
von willebrand disease
|
[NCBI]
|
2.04733e-05
|
|
|
PKD1
|
[NCBI]
|
1.8867e-05
|
|
|
PTHLH
|
[NCBI]
|
1.82948e-05
|
|
|
XDH
|
[NCBI]
|
1.72864e-05
|
|
|
TNC
|
[NCBI]
|
1.45624e-05
|
|
|
BGLAP
|
[NCBI]
|
1.39981e-05
|
|
|
COMP
|
[NCBI]
|
1.13494e-05
|
|
|
EPO
|
[NCBI]
|
1.05451e-05
|
|
|
APOE
|
[NCBI]
|
9.60105e-06
|
|
|
ALB
|
[NCBI]
|
9.302e-06
|
|
|
GIP
|
[NCBI]
|
8.4409e-06
|
|
|
GAPDH
|
[NCBI]
|
4.26878e-06
|
|
|
PTH
|
[NCBI]
|
4.04173e-06
|
|
|
HGF
|
[NCBI]
|
3.57112e-06
|
|
|
MPO
|
[NCBI]
|
2.98892e-06
|
|
|
SPP1
|
[NCBI]
|
2.91977e-06
|
|
|
VEGF
|
[NCBI]
|
1.95857e-06
|
|
|
EGF
|
[NCBI]
|
1.19545e-06
|
|
|
TH
|
[NCBI]
|
8.50116e-07
|
|
|
CRH
|
[NCBI]
|
1.49116e-07
|
|
|
EGFR
|
[NCBI]
|
7.98022e-08
|
|
|
CHAT
|
[NCBI]
|
6.21804e-08
|
|