|
OMIM |
Link |
Information
gain |
01 |
|
|
histiocytosis, familial lipochrome
|
[NCBI]
|
0.00119841
|
|
|
|
r binder deficiency with lactoferrin deficiency
|
[NCBI]
|
0.00098052
|
|
|
|
lymphangiectasia, intestinal
|
[NCBI]
|
0.000898321
|
|
|
|
cryoglobulinemia, familial mixed
|
[NCBI]
|
0.000844965
|
|
|
|
corneal dystrophy, crystalline, of schnyder
|
[NCBI]
|
0.000672238
|
|
|
|
TGD
|
[NCBI]
|
0.000604572
|
|
|
|
TBG
|
[NCBI]
|
0.000572062
|
|
|
|
ALB
|
[NCBI]
|
0.000437389
|
|
|
|
thyroxine-binding globulin of serum
|
[NCBI]
|
0.000341523
|
|
|
|
atransferrinemia
|
[NCBI]
|
0.000174318
|
|
|
|
FGA
|
[NCBI]
|
0.000166837
|
|
|
|
pulmonary fibrosis, idiopathic
|
[NCBI]
|
0.000133758
|
|
|
|
asthma, short stature, and elevated iga
|
[NCBI]
|
0.000125563
|
|
|
|
granulocytopenia with immunoglobulin abnormality
|
[NCBI]
|
0.000125563
|
|
|
|
globulin anomaly involving beta (2a)-globulin
|
[NCBI]
|
0.000125563
|
|
|
|
thrombocytopenia, cyclic
|
[NCBI]
|
0.000103097
|
|
|
|
renal tubular acidosis iii
|
[NCBI]
|
0.000103097
|
|
|
|
immune deficiency, familial variable
|
[NCBI]
|
0.000103097
|
|
|
|
cirrhosis, familial
|
[NCBI]
|
9.46218e-05
|
|
|
|
hypoproteinemia, hypercatabolic
|
[NCBI]
|
9.46218e-05
|
|
|
|
thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis
|
[NCBI]
|
9.46218e-05
|
|
|
|
anemia, autoimmune hemolytic
|
[NCBI]
|
8.17742e-05
|
|
|
|
hyperalphalipoproteinemia
|
[NCBI]
|
7.67499e-05
|
|
|
|
DMPK
|
[NCBI]
|
7.64561e-05
|
|
|
|
F2
|
[NCBI]
|
7.60318e-05
|
|
|
|
PI
|
[NCBI]
|
7.55501e-05
|
|
|
|
elliptocytosis, rhesus-unlinked type
|
[NCBI]
|
7.47252e-05
|
|
|
|
myeloma, multiple
|
[NCBI]
|
6.30741e-05
|
|
|
|
HSAN2
|
[NCBI]
|
6.30741e-05
|
|
|
|
hartnup disorder
|
[NCBI]
|
6.13333e-05
|
|
|
|
RA
|
[NCBI]
|
6.01979e-05
|
|
|
|
FCGRT
|
[NCBI]
|
6.01867e-05
|
|
|
|
HBFQTL1
|
[NCBI]
|
5.90339e-05
|
|
|
|
HIGM1
|
[NCBI]
|
5.08562e-05
|
|
|
|
HAE
|
[NCBI]
|
4.35249e-05
|
|
|
|
HP
|
[NCBI]
|
3.92281e-05
|
|
|
|
CGD
|
[NCBI]
|
3.83862e-05
|
|
|
|
FGG
|
[NCBI]
|
3.8347e-05
|
|
|
|
transcobalamin ii deficiency
|
[NCBI]
|
3.8347e-05
|
|
|
|
complement component 2 deficiency
|
[NCBI]
|
3.63691e-05
|
|
|
|
CYBB
|
[NCBI]
|
3.60174e-05
|
|
|
|
wilson disease
|
[NCBI]
|
3.38432e-05
|
|
|
|
HBD
|
[NCBI]
|
3.35852e-05
|
|
|
|
A2M
|
[NCBI]
|
3.20928e-05
|
|
|
|
SMAX1
|
[NCBI]
|
2.96253e-05
|
|
|
|
B2M
|
[NCBI]
|
2.93102e-05
|
|
|
|
CMH
|
[NCBI]
|
2.90118e-05
|
|
|
|
HS
|
[NCBI]
|
2.80211e-05
|
|
|
|
factor v deficiency
|
[NCBI]
|
2.63661e-05
|
|
|
|
SERPINA6
|
[NCBI]
|
2.35468e-05
|
|
|
|
homocystinuria
|
[NCBI]
|
2.30905e-05
|
|
|
|
BCHE
|
[NCBI]
|
2.26557e-05
|
|
|
|
dystrophia myotonica 1
|
[NCBI]
|
2.25057e-05
|
|
|
|
MAG
|
[NCBI]
|
1.70304e-05
|
|
|
|
TF
|
[NCBI]
|
1.15305e-05
|
|
|
|
APOB
|
[NCBI]
|
8.17332e-06
|
|
|
|
TTR
|
[NCBI]
|
7.9505e-06
|
|
|
|
TG
|
[NCBI]
|
3.69749e-06
|
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
2.68569e-06
|
|
