|
OMIM |
Link |
Information gain |
01 |
|
cryoglobulinemia, familial mixed
|
[NCBI]
|
0.0109258
|
|
|
SLE
|
[NCBI]
|
0.000782998
|
|
|
cryofibrinogenemia, familial primary
|
[NCBI]
|
0.000130109
|
|
|
factor viii deficiency
|
[NCBI]
|
0.000118204
|
|
|
anemia, autoimmune hemolytic
|
[NCBI]
|
0.000110479
|
|
|
RA
|
[NCBI]
|
9.11121e-05
|
|
|
von willebrand disease
|
[NCBI]
|
8.75192e-05
|
|
|
autoimmune disease
|
[NCBI]
|
8.34499e-05
|
|
|
von willebrand disease, recessive form
|
[NCBI]
|
8.34499e-05
|
|
|
factor xii deficiency
|
[NCBI]
|
7.27425e-05
|
|
|
TTP
|
[NCBI]
|
6.73835e-05
|
|
|
FCAS
|
[NCBI]
|
6.0856e-05
|
|
|
HAE
|
[NCBI]
|
4.91969e-05
|
|
|
MAG
|
[NCBI]
|
3.98646e-05
|
|
|
ALB
|
[NCBI]
|
3.68179e-05
|
|
|
complement component 6 deficiency
|
[NCBI]
|
3.00591e-05
|
|
|
protein c deficiency, congenital thrombotic disease due to
|
[NCBI]
|
2.60166e-05
|
|
|
IFNA1
|
[NCBI]
|
2.23014e-05
|
|
|
TNF
|
[NCBI]
|
1.3831e-06
|
|