CP, ceruloplasmin, 1356

N. diseases: 283; N. variants: 64
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Familial apoceruloplasmin deficiency
disease Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 2 0.300 None 1.000 3 2003 2012
HEMOSIDEROSIS, SYSTEMIC, DUE TO ACERULOPLASMINEMIA
disease Nutritional and Metabolic Diseases Disease or Syndrome 1 3 0.300 None 1.000 3 3 1999 2008
CUI: C1527352
Disease: Hepatic Form of Wilson Disease
Hepatic Form of Wilson Disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 24 0.300 None 1.000 3 1994 2013
CUI: C0022116
Disease: Ischemia
Ischemia
phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 103 0.300 None 1.000 2 2005 2007
CUI: C0221169
Disease: Hemiballismus
Hemiballismus
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 9 0.300 None 1.000 1 2003 2003
CUI: C0023904
Disease: Liver Neoplasms, Experimental
Liver Neoplasms, Experimental
phenotype Digestive System Diseases; Neoplasms Neoplastic Process; Experimental Model of Disease 152 0.300 None 1.000 1 2013 2013
CUI: C0338630
Disease: Senile Paranoid Dementia
Senile Paranoid Dementia
disease Nervous System Diseases; Mental Disorders Mental or Behavioral Dysfunction 8 0.300 None 1.000 1 2003 2003
CUI: C0232766
Disease: Asterixis
Asterixis
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 7 0.300 None 1.000 1 2003 2003
CUI: C0240991
Disease: Ataxia, Sensory
Ataxia, Sensory
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 35 1 0.300 None 1.000 1 2003 2003
CUI: C0022660
Disease: Kidney Failure, Acute
Kidney Failure, Acute
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 826 32 0.300 None 1.000 1 2017 2017
CUI: C0278161
Disease: Ataxia, Motor
Ataxia, Motor
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Finding 16 0.300 None 1.000 1 2003 2003
CUI: C0085397
Disease: Pasteurellaceae Infections
Pasteurellaceae Infections
group Infections Disease or Syndrome 3 0.300 None 1.000 1 2006 2006
CUI: C0041755
Disease: Adverse reaction to drug
Adverse reaction to drug
group Chemically-Induced Disorders Pathologic Function 87 0.300 None 1.000 1 2017 2017
CUI: C0019208
Disease: Hepatoma, Novikoff
Hepatoma, Novikoff
disease Digestive System Diseases; Neoplasms Neoplastic Process; Experimental Model of Disease 125 0.300 None 1.000 1 2013 2013
CUI: C0019207
Disease: Hepatoma, Morris
Hepatoma, Morris
disease Digestive System Diseases; Neoplasms Neoplastic Process; Experimental Model of Disease 124 0.300 None 1.000 1 2013 2013
CUI: C0524611
Disease: Cryptogenic Chronic Hepatitis
Cryptogenic Chronic Hepatitis
disease Digestive System Diseases Disease or Syndrome 22 0.300 None 1.000 1 2015 2015
CUI: C0342302
Disease: Brittle diabetes
Brittle diabetes
disease Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases Disease or Syndrome 44 0.300 None 1.000 1 2010 2010
CUI: C0019193
Disease: Hepatitis, Toxic
Hepatitis, Toxic
disease Digestive System Diseases; Chemically-Induced Disorders Injury or Poisoning 412 0.300 None 1.000 1 2014 2014
CUI: C0520966
Disease: Abnormal coordination
Abnormal coordination
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Finding 59 4 0.300 None 1.000 1 2003 2003
CUI: C0454606
Disease: Oral Dyskinesia
Oral Dyskinesia
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 7 0.300 None 1.000 1 2003 2003
CUI: C0025202
Disease: melanoma
melanoma
disease Neoplasms Neoplastic Process 3087 515 0.300 None 1.000 1 2013 2013
CUI: C0427190
Disease: Ataxia, Truncal
Ataxia, Truncal
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 68 13 0.300 None 1.000 1 2003 2003
CUI: C0027746
Disease: Nerve Degeneration
Nerve Degeneration
phenotype Pathological Conditions, Signs and Symptoms Cell or Molecular Dysfunction 165 17 0.300 None 1.000 1 2008 2008
CUI: C0085584
Disease: Encephalopathies
Encephalopathies
group Nervous System Diseases Disease or Syndrome 457 64 0.300 None 1.000 1 2009 2009
CUI: C0971858
Disease: Arthritis, Collagen-Induced
Arthritis, Collagen-Induced
disease Musculoskeletal Diseases Experimental Model of Disease 43 0.300 None 1.000 1 2009 2009