Source: ALL

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 1356
Gene Symbol: CP
CP
ceruloplasmin 0.466 0.846 4.2E-10
CUI: C0878682
Disease: Ceruloplasmin deficiency
Ceruloplasmin deficiency
disease 0.900 None 1.000 42 51 1987 2019
Entrez Id: 1356
Gene Symbol: CP
CP
ceruloplasmin 0.466 0.846 4.2E-10
CUI: C0012715
Disease: Iron Metabolism Disorders
Iron Metabolism Disorders
group 0.530 None 1.000 5 0 1998 2006
Entrez Id: 1356
Gene Symbol: CP
CP
ceruloplasmin 0.466 0.846 4.2E-10
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
group 0.460 None 1.000 7 2 1995 2017
Entrez Id: 1356
Gene Symbol: CP
CP
ceruloplasmin 0.466 0.846 4.2E-10
CUI: C0497327
Disease: Dementia
Dementia
disease 0.410 None 1.000 2 0 2003 2015
Entrez Id: 1356
Gene Symbol: CP
CP
ceruloplasmin 0.466 0.846 4.2E-10
CUI: C0019202
Disease: Hepatolenticular Degeneration
Hepatolenticular Degeneration
disease 0.400 None 0.906 53 1 1987 2020
Entrez Id: 1356
Gene Symbol: CP
CP
ceruloplasmin 0.466 0.846 4.2E-10
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
disease 0.400 None 0.938 16 0 2004 2020
Entrez Id: 1356
Gene Symbol: CP
CP
ceruloplasmin 0.466 0.846 4.2E-10
CUI: C0282193
Disease: Iron Overload
Iron Overload
disease 0.400 None 1.000 13 0 2000 2019
Entrez Id: 1356
Gene Symbol: CP
CP
ceruloplasmin 0.466 0.846 4.2E-10
CUI: C0035304
Disease: Retinal Degeneration
Retinal Degeneration
phenotype 0.400 None 1.000 1 0 2003 2003
Entrez Id: 1356
Gene Symbol: CP
CP
ceruloplasmin 0.466 0.846 4.2E-10
CUI: C0004134
Disease: Ataxia
Ataxia
phenotype 0.400 None 1.000 1 0 2003 2003
Entrez Id: 1356
Gene Symbol: CP
CP
ceruloplasmin 0.466 0.846 4.2E-10
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
disease 0.330 None 1.000 4 0 2002 2018
Entrez Id: 1356
Gene Symbol: CP
CP
ceruloplasmin 0.466 0.846 4.2E-10
Diabetes Mellitus, Insulin-Dependent
disease 0.330 None 1.000 4 0 1996 2019
Entrez Id: 1356
Gene Symbol: CP
CP
ceruloplasmin 0.466 0.846 4.2E-10
CUI: C0022716
Disease: Menkes Kinky Hair Syndrome
Menkes Kinky Hair Syndrome
disease 0.330 None 1.000 3 0 1981 2012
Entrez Id: 1356
Gene Symbol: CP
CP
ceruloplasmin 0.466 0.846 4.2E-10
CUI: C0018995
Disease: Hemochromatosis
Hemochromatosis
disease 0.320 None 1.000 3 0 2003 2007
Entrez Id: 1356
Gene Symbol: CP
CP
ceruloplasmin 0.466 0.846 4.2E-10
CUI: C0392514
Disease: Hereditary hemochromatosis
Hereditary hemochromatosis
disease 0.320 None 1.000 3 0 2001 2007
Entrez Id: 1356
Gene Symbol: CP
CP
ceruloplasmin 0.466 0.846 4.2E-10
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis
disease 0.310 None 1.000 3 0 2014 2018
Entrez Id: 1356
Gene Symbol: CP
CP
ceruloplasmin 0.466 0.846 4.2E-10
CUI: C0239946
Disease: Fibrosis, Liver
Fibrosis, Liver
disease 0.310 None 1.000 3 0 2014 2018
Entrez Id: 1356
Gene Symbol: CP
CP
ceruloplasmin 0.466 0.846 4.2E-10
CUI: C0009375
Disease: Colonic Neoplasms
Colonic Neoplasms
group 0.310 None 1.000 2 0 2003 2013
Entrez Id: 1356
Gene Symbol: CP
CP
ceruloplasmin 0.466 0.846 4.2E-10
CUI: C0520463
Disease: Chronic active hepatitis
Chronic active hepatitis
disease 0.310 None 1.000 2 0 1980 2015
Entrez Id: 1356
Gene Symbol: CP
CP
ceruloplasmin 0.466 0.846 4.2E-10
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
disease 0.310 None 1.000 2 0 2013 2016
Entrez Id: 1356
Gene Symbol: CP
CP
ceruloplasmin 0.466 0.846 4.2E-10
CUI: C0427086
Disease: Involuntary Movements
Involuntary Movements
phenotype 0.310 None 1.000 2 0 2001 2003
Entrez Id: 1356
Gene Symbol: CP
CP
ceruloplasmin 0.466 0.846 4.2E-10
CUI: C0019189
Disease: Hepatitis, Chronic
Hepatitis, Chronic
disease 0.310 None 1.000 2 0 2010 2015
Entrez Id: 1356
Gene Symbol: CP
CP
ceruloplasmin 0.466 0.846 4.2E-10
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
disease 0.310 None 1.000 2 0 2000 2009
Entrez Id: 1356
Gene Symbol: CP
CP
ceruloplasmin 0.466 0.846 4.2E-10
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
disease 0.310 None 1.000 2 0 2002 2004
Entrez Id: 1356
Gene Symbol: CP
CP
ceruloplasmin 0.466 0.846 4.2E-10
CUI: C0013421
Disease: Dystonia
Dystonia
phenotype 0.310 None 1.000 2 0 1987 2006
Entrez Id: 1356
Gene Symbol: CP
CP
ceruloplasmin 0.466 0.846 4.2E-10
CUI: C0032914
Disease: Pre-Eclampsia
Pre-Eclampsia
phenotype 0.310 None 1.000 1 0 2008 2008