Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Hypoproteinemia [NCBI]

Gene


 Gene Link Information
Gain		 01
FCGRT [NCBI] 1.63495e-05
SERPINA7 [NCBI] 1.55699e-05
SLC25A13 [NCBI] 1.19779e-05
B2M [NCBI] 1.04325e-05
NPHS1 [NCBI] 8.90706e-06
TJP1 [NCBI] 8.88153e-06
ALB [NCBI] 8.20497e-06
CCK [NCBI] 6.51493e-06
PRL [NCBI] 4.99688e-06
EGF [NCBI] 4.16792e-06



OMIM


 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



Database Center for Life Science