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01 Blood Protein Disorders [NCBI]


Gene


Gene Link Information
Gain
01
ALB [NCBI] 1.69876e-05
HDLBP [NCBI] 1.02825e-05
HBD [NCBI] 1.02079e-05
PROC [NCBI] 9.46845e-06
LCAT [NCBI] 9.10016e-06
TF [NCBI] 7.13708e-06
F2 [NCBI] 6.76881e-06
TTR [NCBI] 6.75588e-06
TRH [NCBI] 5.63364e-06
TG [NCBI] 5.55767e-06
VWF [NCBI] 4.35194e-06




OMIM


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




Database Center for Life Science