|
OMIM |
Link |
Information gain |
01 |
|
spondyloepiphyseal dysplasia tarda, autosomal recessive
|
[NCBI]
|
0.00115589
|
|
|
lymphangiectasia, intestinal
|
[NCBI]
|
0.00107364
|
|
|
hypoproteinemia, hypercatabolic
|
[NCBI]
|
0.000255404
|
|
|
enterokinase deficiency
|
[NCBI]
|
0.000218479
|
|
|
JBS
|
[NCBI]
|
0.00017481
|
|
|
pancreatic insufficiency, combined exocrine
|
[NCBI]
|
0.000142554
|
|
|
TBG
|
[NCBI]
|
0.00012031
|
|
|
thyroxine-binding globulin of serum
|
[NCBI]
|
0.000106098
|
|
|
B2M
|
[NCBI]
|
0.00010083
|
|
|
pancreatic agenesis, congenital
|
[NCBI]
|
9.37095e-05
|
|
|
atransferrinemia
|
[NCBI]
|
9.16802e-05
|
|
|
complement component 5 deficiency
|
[NCBI]
|
8.82563e-05
|
|
|
aceruloplasminemia
|
[NCBI]
|
8.19513e-05
|
|
|
FCGRT
|
[NCBI]
|
7.40637e-05
|
|
|
ABL
|
[NCBI]
|
5.99797e-05
|
|
|
PRSS1
|
[NCBI]
|
5.17404e-05
|
|
|
C3
|
[NCBI]
|
4.79322e-05
|
|
|
DMPK
|
[NCBI]
|
4.49747e-05
|
|
|
homocystinuria
|
[NCBI]
|
3.6694e-05
|
|
|
PI
|
[NCBI]
|
2.78364e-05
|
|
|
ALB
|
[NCBI]
|
2.45325e-05
|
|
|
APOB
|
[NCBI]
|
2.05843e-05
|
|
|
CCK
|
[NCBI]
|
1.44903e-05
|
|
|
CF
|
[NCBI]
|
6.89512e-06
|
|
|
PRL
|
[NCBI]
|
6.78046e-06
|
|
|
EGF
|
[NCBI]
|
3.56537e-06
|
|